| Literature DB >> 29744363 |
Reinie Cordier1, Brandon Vilaysack2, Kenji Doma2, Sarah Wilkes-Gillan3, Renée Speyer1,4,5.
Abstract
OBJECTIVE: To assess the effectiveness of peer inclusion in interventions to improve the social functioning of children with ADHD.Entities:
Mesh:
Year: 2018 PMID: 29744363 PMCID: PMC5878915 DOI: 10.1155/2018/7693479
Source DB: PubMed Journal: Biomed Res Int Impact factor: 3.411
Full electronic search strategy.
| Database | Search terms | Limitations | Results | |
|---|---|---|---|---|
| Subject headings | CINAHL | (MH “Attention Deficit Hyperactivity Disorder”) AND ((MH “Peer Group”) OR (MH “Peer Counseling”) OR (MH “Peer Review”) OR (MH “Friendship”) OR (MH “Psychotherapy, Group”) OR (MH “Group Processes”) OR (MH “Support Groups”) OR (MH “Role Playing”) OR (MH “Play Therapy”) OR (MH “Camps”) OR (MH “Social Skills Training”) OR (MH “Social Skills”) OR (MH “Communication Skills Training”) OR (MH “Students, High School”) OR (MH “Schools, Middle”) OR (MH “Schools, Special”) OR (MH “Schools, Secondary”) OR (MH “Schools, Elementary”) OR (MH “Social Behavior”)) | Age: child, preschool: 2–5 years; child: 6–12 years; adolescent: 13–18 years | 280 |
| Embase | (Attention deficit disorder/) AND (peer rejection/OR “peer review”/OR peer acceptance/or peer counseling/OR peer group/OR friendship/OR play/OR play therapy/OR group therapy/OR social adaptation/OR social behavior/OR social interaction/) | Age: preschool child <1 to 6 years>; school child <7 to 12 years>; adolescent <13 to 17 years> | 1296 | |
| Medline | (attention deficit disorder with hyperactivity/) AND (Friends/OR Psychotherapy, Group/OR play therapy/OR social behavior/) | Age: preschool child (2 to 5 years); child (6 to 12 years); adolescent (13 to 18 years) | 505 | |
| PsycINFO | (DE “Attention Deficit Disorder with Hyperactivity”) AND (DE (“peer counselling”) OR DE (“peer tutoring”) or DE (“peers”) OR DE (“peer evaluation”) OR DE (“friendship”) OR DE (“group intervention”) OR DE (“group participation”) OR DE (“group psychotherapy”) OR DE (“group dynamics”) OR DE (“group cohesion”) OR DE (“group participation”) OR DE (“childhood play behavior”) OR DE (“childhood play development”) OR DE (“play therapy”) OR DE (“therapeutic camps”) OR DE (“school based intervention”) OR DE (“psychosocial development”) OR DE (“psychosocial factors”) OR DE (“psychosocial readjustment”) OR DE (“psychosocial rehabilitation”) OR DE (“social skills”) OR DE (“social skills training”) OR DE (“social group work”) OR DE (“social groups”) OR DE (“social integration”) OR DE (“social interaction”) OR DE (“Social behaviour”) OR DE (“group counseling”)) | Age: preschool age <age 2 to 5 yrs>; school age <age 6 to 12 yrs>; adolescence <age 13 to 17 yrs> | 737 | |
|
| ||||
| Free text words | CINAHL | (ADHD OR ADD OR “Attention deficit hyperactivity disorder”) AND (peer | Published date: 20151101–20161131 | 280 |
| Embase |
| Last year | 177 | |
| Medline |
| Published date: 2016 - Current | 97 | |
| PSYCINFO |
| Published date: 20151101–20161131 | 365 | |
Figure 1Flow diagram of the reviewing process according to PRISMA [115].
Reasons for exclusion of papers published in peer reviewed journals.
| Study | Reason for exclusion |
|---|---|
| Antshel [ | No intervention |
| Arnett et al. [ | No intervention |
| Erhardt and Hinshaw [ | No intervention |
| Haas and Waschbusch [ | No intervention |
| Landau and Moore [ | No intervention |
| Mikami and Hinshaw [ | No intervention |
| Mikami and Huang-Pollock [ | No intervention |
|
| |
| Antshel [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Burrows [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Charlebois [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Evans and Schultz [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Frame [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Frame et al. [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Gardner [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Gerber et al. [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Gerber-von Müller et al. [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Langberg [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Mikami et al. [ | Not peer inclusion—description of intervention did not include peer inclusion component |
| Abdollahian et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Abikoff et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Antshel and Remer [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Hariri and Faisal [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Jans et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Jans et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Looyeh et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
| Tutty et al. [ | Not peer inclusion—study assessed ADHD symptoms with no social skills outcomes |
|
| |
| Burrows [ | Peer inclusion—no social skills outcomes |
| DuPaul et al. [ | Peer inclusion—no social skills outcomes |
| Gol and Jarus [ | Peer inclusion—no social skills outcomes |
| Hechtman et al. [ | Peer inclusion—no social skills outcomes |
| O'Connor et al. [ | Peer inclusion—no social skills outcomes |
| Power et al. [ | Peer inclusion—no social skills outcomes |
| Rickson and Watkins [ | Peer inclusion—no social skills outcomes |
| Storebø et al. [ | Peer inclusion—no social skills outcomes |
|
| |
| Cantrill et al. [ | No comparison group |
| Wilkes et al. [ | No comparison group |
| Wilkes-Gillan et al. [ | No comparison group |
| Wilkes-Gillan et al. [ | No comparison group |
|
| |
| Storebø et al. [ | Protocol paper |
|
| |
| Schmitman Gen Pothmann et al. [ | Non-English |
| Tabaeian [ | Non-English |
Note. Table does not include seven excluded dissertations and one excluded conference abstract.
Peer included studies for children with ADHD.
| Design | Treatment condition | Participants N | Age Years (mean ± SD) | Inclusion criteria | Outcome measurea | Treatment outcome |
|---|---|---|---|---|---|---|
| Abikoff et al. [ | 1 year weekly, 2nd year monthly | mph: 34 (ADHD) | 8.2 ± 0.8 | ADHD diagnosis |
| SSRS: significant improvement |
|
| ||||||
| Choi and Lee [ | Weekly EMT and SST treatment for 16 weeks | EMT: 25 | EMT: | ADHD diagnosis |
| No differences between SST and control groups. EMT group improved significantly more than control |
|
| ||||||
| Frankel et al. [ | SST weekly for 12 weeks | Treatment | 9.05 ± 3.06 | Peer problems |
| SSRS: significantly greater improvement |
|
| ||||||
| Guli et al. [ | SST weekly for 12 weeks or twice weekly for 8 weeks | SCIP: 18 (5 ADHD/2 NLD/11 ASD) | 10.97 ± 1.98 | ADHD diagnosis |
| BASC: no significant effects found |
|
| ||||||
| Haas et al. [ | Behavioural treatment for 8 weeks in the context of a STP | Treatment | 9.48 ± 1.58 | ADHD diagnosis |
| SIRF: significant improvement in social skills and problem solving |
|
| ||||||
| Hannesdottir et al. [ | Behavioural and SST treatment with working memory training | Treatment: 16 | 9.2 ± 0.62 | ADHD diagnosis |
| Significant group × time interactions favouring treatment group over waitlist control |
|
| ||||||
| Hantson et al. [ | SST daily for 2 weeks in the context of an intensive therapeutic summer day camp | Treatment | 8.6 ± 1.6 | ADHD diagnosis |
| IPR: significant improvement |
|
| ||||||
| Huang et al. [ | Weekly SST treatment for 8 weeks consisting of 80-minute sessions | SST: 45 | SST: | ADHD diagnosis |
| SSRS-C: significant improvement in Self-Control in favour of SST group; SSRS-T: significant improvement in active participation in favour of SST group |
|
| ||||||
| Jensen et al. [ | Treatment over 14 months | Medication management | 11.8 ± 0.95 | Children who participated in the 1999 MTA study |
| SSRS: effect size for improvement from baseline to 36 months across all treatment groups was 0.8–0.9 |
|
| ||||||
| Kolko et al. [ | 3 weekly sessions for 5 weeks | SCST: 36 (10 ADHD/11 CD/15 OD) | 10.4 ± 2.1 | Score of at least 7 on a four-item social problems screen, with at least one maximum rating |
| CAI-M: significant improvement in post-training scores |
|
| ||||||
| Mikami et al. [ | Weekdays for four weeks total | MOSAIC: 12 ADHD/58 TD | 8.15 ± 0.79 | ADHD diagnosis after screening |
| Main effect on positive nominations for treatment was not significant. Received fewer negative nominations and more reciprocated friendship nominations when in MOSAIC relative to COMET group |
|
| ||||||
| MTA Cooperative Group [ | Treatment over 14 months | Medication management | 8.5 ± 0.8 | ADHD combined type diagnosis |
| SSRS: significant improvement for parent-reported internalizing problems for combined treatment over behavioural treatment |
|
| ||||||
| MTA Cooperative Group [ | Treatment over 14 months | Medication management | 8.4 ± 0.8 | Children who participated in the 1999 MTA study |
| SSRS: nonsignificant overall treatment effect |
|
| ||||||
| Pfiffner et al. [ | Treatment over 12 weeks | Five cohorts of children randomized to either CLAS program or control | 8.7 ± 1.2 | ADHD diagnosis |
| SSRS: significant improvements |
|
| ||||||
| Shechtman and Katz [ | Weekly for 15 weeks | Group Therapy: 42 (20: ADD or ADHD/22 LD) | 13.26 ± 0.77 | ADD/ADHD or LD diagnosis |
| Significant treatment condition by time effect |
|
| ||||||
| Storebø et al. [ | Weekly for 8 weeks | Experimental treatment | 10.4 ± 1.31 | ADHD diagnosis | Indexes from Conners 3 and Connors CBRS: | No statistically significant difference when comparing groups |
|
| ||||||
| Waxmonsky et al. [ | Weekly for 8 weeks | Atomoxetine + BT | 8.59 ± 1.58 | ADHD diagnosis |
| SSRS: significantly lower parent-rated problem behaviours |
Notes. RCT = randomized controlled trial, QES = quasi-experimental study, mph = methylphenidate, MPT = Multipsychosocial Treatment, SST = social skills training, ACT = attention control treatment, ADHD = Attention-Deficit Hyperactivity Disorder, SSRS =Social Skills Rating Scale [70], TOPS =Taxonomy of Problem Situations [71], EMT = emotional management training, WISC-Revised Korean Version = Wechsler Intelligence Scale for Children-Revised Korean Version [72], CBCL = Child Behaviour Checklist [73, 74], ODD = oppositional defiant disorder, DSM-III-R = Diagnostic and Statistical Manual of Mental Disorders 3rd Edition, PEI = Pupil Evaluation Inventory [75], SCIP = Social Competence Intervention Program, NLD = nonverbal learning disorder, ASD = autism spectrum disorder, WISC-III (Weschler Intelligence Scale for Children-III [76]), BASC = Behaviour Assessment System for Children [77], DANVA2 = Diagnostic Analysis of Nonverbal Accuracy 2 Nowicki, 2004, CP = conduct problems, SIRF = Staff Improvement Rating Form [78], ERC = Emotion Regulation Checklist [79]; SDQ = Strengths and Difficulties Questionnaire [80], Icelandic WISC-IV = Wechsler Intelligence Scale for Children-Icelandic version [81], IPR = Index of Peer Relations [82], WFIRS-P = Weiss Functional Impairment Rating Scale-Parent Version [83], CGI-P = Conners' Global Index-Parent Version [84], SNAP = (Swanson, Nolan, and Pelham Rating Scale [85], STP = summer treatment program, MTA = Multimodal Treatment Study of Children with ADHD, WIAT = Wechsler Individual Achievement Test [86], CIS = Columbia Impairment Scale [87], SCST = social-cognitive skills training, SA = social activity group, CD = conduct disorder, OD = other disorders, CAI-M = Children's Assertiveness Inventory-Modified [88], LNS-M = Loneliness Scale for Children-Modified [89], SPS = Social Problems Screen, MOSAIC = Making Socially Accepting Inclusive Classrooms, COMET = contingency management training, TD = typically developing, WASI = Wechsler Abbreviated Scale of Intelligence [90], MASC = Multidimensional Anxiety Scale for Children [91], CLAS = Child Life and Attention Skills program, SCT Scale = Sluggish Cognitive Tempo Scale [92], COSS = Children's Organizational Scale [93], DSM-IV = Diagnostic and Statistical Manual of Mental Disorders 4th Edition, LD = learning disabilities, Conners 3 [94], Conners CBRS = Conners Behaviour Rating Scales [94], BT = behaviour therapy, DBD = Disruptive Behaviour Disorders Rating Scale [95], APRS = Academic Performance Rating Scale [96], PSERS = Pittsburgh Side Effects Rating Scale [97], CDRS-R = Children's Depression Rating Scale-Revised [98], and DRC/ITBE = Daily Report Card/Individual Target Behaviour Evaluation. aWhen handling studies with multiple social skills outcome measures, one singular outcome measure was chosen that most comprehensively reflected the construct social skills. This singular outcome measure was then used for the calculation of an effect size. No measures were aggregated within the study to obtain one effect size.
Intervention components of included studies.
| Study | Peer component | Parent component | Teacher component | Skills | Medication |
|---|---|---|---|---|---|
| Frankel et al. [ | Children were didactically presented social skills and required to rehearse behaviours between each other. Participants were also taught conversational techniques and rehearsed them in the context of introductions to other class members | (i) Parent sessions | (i) Teacher ratings of antisocial, prosocial, and aggressive behaviour | (i) Conversation | All ADHD participants were required to take medication (incl. methylphenidate, dextroamphetamine, pemoline, other psychotropic medication) |
|
| |||||
| Guli et al. [ | The sessions included activities that focus on establishing social skills through several improvisations or process dramas, through which they practice perspective taking and cognitive flexibility with their peers. | (i) Parent ratings of social skills | (i) None | (i) Group cohesion | 51.3% of participants were reported to take prescription medication. Treatment: 12 medication & 6 no medication; Control: 4 medication & 12 no medication |
|
| |||||
| Haas et al. [ | Counsellor-led questions prompted a discussion of the social skills by encouraging children to provide a description of the social skills (e.g., definition, examples) and to model and role-play good and bad examples of how to use the social skill. | (i) Parent ratings of ADHD, ODD, and CD symptoms | (i) None | Social skills: | All ADHD participants were either not taking medication or prescribed a placebo assignment. However, some children were on medication for some (but not all) days during the summer treatment program |
|
| |||||
| Hantson et al. [ | The therapist first described how to perform the skills in an appropriate manner. The children were then paired and asked to role-play the new skill in front of the group. Following this, children were asked to role-play the skills from the other's perspective in an effort to understand situations from other person's point of view. | (i) Parent psychoeducation and training | (i) None | Social skills: | Participants who were on medication stayed on medication; those who were not on medication remained so. Treatment: 20 medication & 13 no medication; control: 9 medication & 6 no medication |
|
| |||||
| Huang et al. [ | Children were taught various social skill modules via didactic instructions, modelling, role-play activities and behavioural rehearsals | (i) Weekly parent sessions to educate on ADHD | Teacher ratings of attention, hyperactivity, impulsivity, oppositional, cooperative behaviour, self-assertion, self-control and conflict coping | (i) Conversation | All ADHD participants received methylphenidate with drug compliance controlled |
|
| |||||
| Kolko et al. [ | Cotherapists and children engaged in several role-plays. The group discussed each role-play and provided constructive performance feedback. Inadequate role-plays were rehearsed a second time to promote mastery. | (i) None | (i) One-year follow-up teacher ratings of social skills and outcome measures | (i) Social involvement | Comparable percentages of children in SCST and SA groups received methylphenidate (22% versus 20%), imipramine (11% versus 10%), lithium (8% versus 5%), or other medications (7% versus 5%) |
|
| |||||
| Abikoff et al. [ | Peers role-played and modelled appropriate and inappropriate social behaviours in groups of four. | (i) Parent training | (i) Teacher ratings of socially rejected and accepted children | (i) Basic interaction skills | All participants were prescribed methylphenidate after a 5-week clinical methylphenidate trial and placebo substitution to determine positive response to medication prior to treatment |
|
| |||||
| Choi and Lee [ | EMT: children undertook activities that covered four major behavioural characteristics: (1) identification and labelling of emotional words; (2) emotional recognition and expression; (3) emotional understanding; and (4) emotional regulation in social situations | (i) Parent ratings on emotional and behavioural problems in children | Interacted with children as part of the SST and EMT programs | (i) Basic interaction skills | All participants were prescribed with medication during the course of the study although not controlled |
|
| |||||
| Hannesdottir et al. [ | Therapists lead discussions amongst groups of three children to aid solving problems presented at a number of “stations.” Stations included the Emotion Station, Friendship Station, Stopping Station, and Problem-Solving Station. In addition, there was a Brain Training Station, at which children practiced computer-based executive function tasks. | (i) Parent ratings of social skills | None | (i) Identifying facial expressions | 100% of participants in treatment group were on medication for the duration of the study. There were 12 participants on medication in the control group (85.7%) at study commencement, dropping to 11 participants at the end of the study (78.6%) |
|
| |||||
| Jensen et al. [ | Sessions include instruction, modelling, role-playing and practice in key social concepts such as communication, as well as more specific skills. In addition to these sessions, the children engaged in a daily cooperative group task that is designed to promote cooperation and contribute to cohesive peer relationships. A buddy system was employed to help children develop individual friendships that may “buffer” them from the possible negative effects of being unpopular. This was accomplished by assigning each child a buddy with whom their goal is to form a close friendship. The children engage in a variety of activities with their buddies and meet regularly with adult “buddy coaches” who assist them in working out relationship problems. | (i) Parent training | School-based treatment: | (i) Social skills effective for peer group functioning | 71% of combined treatment and medication management participants were using medication at high levels compared to 62% and 45% of community care and behavioural treatment participants, respectively. Average medication doses differed across all groups |
|
| |||||
| Mikami, Griggs [ | Peers were trained to be more socially inclusive in the MOSAIC treatment condition. Teachers assigned children to work in teams for collaborative activities where children had to work together in order to succeed. | (i) None | (i) Summer program teacher ratings of problem behaviours | (i) Social skills | 10 out of 24 children with ADHD were medicated with psychotropic medication, and some were taking additional medications for comorbid conditions. All medicated children stayed on a consistent regimen during the summer program |
|
| |||||
| The MTA Cooperative Group [ | Sessions included instruction, modelling, role-playing, and practice in key social concepts such as communication, as well as more specific skills. In addition to these sessions, the children engaged in a daily cooperative group task that was designed to promote cooperation and contribute to cohesive peer relationships. A Buddy System was employed to help children develop individual friendships that may “buffer” them from the possible negative effects of being unpopular. This was accomplished by assigning each child a buddy with whom their goal is to form a close friendship. The children engaged in a variety of activities with their buddies and met regularly with adult “buddy coaches” who assisted them in working out relationship problems. | (i) Parent training | School-based treatment: | (i) Social skills effective for peer group functioning | All participants in the treatment groups were prescribed medication, however 3.1% of the combined treatment and medication management subjects were on no medication |
|
| |||||
| MTA Cooperative Group [ | Sessions included instruction, modelling, role-playing, and practice in key social concepts such as communication, as well as more specific skills. In addition to these sessions, the children engaged in a daily cooperative group task that was designed to promote cooperation and contribute to cohesive peer relationships. A Buddy System was employed to help children develop individual friendships that may “buffer” them from the possible negative effects of being unpopular. This was accomplished by assigning each child a buddy with whom their goal is to form a close friendship. The children engaged in a variety of activities with their buddies and met regularly with adult “buddy coaches” who assisted them in working out relationship problems. | (i) Parent training | School-based treatment: | (i) Social skills effective for peer group functioning | 70% of combined treatment and 72% of medication management participants were using medication at high levels compared to 62% and 38% of community care and behavioural treatment, respectively |
|
| |||||
| Pfiffner et al. [ | Children role-played the positive use of a skill, using brief scripts of common problem situations with peers or siblings (e.g., entering a game, getting out during a game, and being teased). Children evaluated each other's performance of the social skills immediately after each role-play and were called on to give specific reasons for their ratings. | (i) Parent training | (i) Teacher consultation | (i) Social competence | Children were excluded if they changed medication status during the course of the study. Only two subjects (both in CLAS program group) began the study taking medication (atomoxetine); they continued medication at posttreatment and follow-up. Two children in the control group began medication at posttreatment, and one did so at follow-up |
|
| |||||
| Shechtman and Katz [ | The expressive-supportive modality uses an integrative theoretical approach in therapy, with a strong emphasis on self-expressiveness and group support. Activities and therapeutic games are consistently used to help participants function in the group process. | (i) None | (i) None | (i) Initiation | No mention of whether participants were medicated or nonmedicated |
|
| |||||
| Storebø et al. [ | Different methods of teaching the children were used. These include didactic instructions, work with symbols (e.g., dolls), role-play, creative techniques, physical exercises, music, story reading, games, and movies. Each session had a theme of a particular aspect of social skills training. | (i) Parent training | (i) Teacher ratings of academic and behavioural performance, social problems, peer relations and emotional regulation | (i) Self-worth | All participants were prescribed medication. Treatment started with the first choice: methylphenidate; the second choice: dexamphetamine; and atomoxetine if significant anxiety component change or suspicion of dexamphetamine abuse |
|
| |||||
| Waxmonsky et al. [ | Each session began with a brief description of the social skills of the day, which was presented to the child didactically and through modelling and role-playing. | (i) Parent training | (i) Teacher implemented daily report card | (i) Cooperation | All participants were prescribed atomoxetine |
Notes. QES = quasi-experimental study; RCT = randomized controlled trial; ADHD = attention-deficit/hyperactivity disorder; ODD = oppositional defiant disorder; CD = conduct disorder; SCST = social-cognitive skills training; SA = social activity; EMT = emotional management training; SST = social skills training; MOSAIC = Making Socially Accepting Inclusive Classrooms; and CLAS = Child Life and Attention Skills program.
Methodological quality of included studies.
| Study | Treatment | Control | NHMRC evidence level | Randomization | Blinding | Methodological quality |
|---|---|---|---|---|---|---|
| Abikoff et al. [ | Child and parent training with medication | Attention control with medication | II | Block randomization scheme with blocks of 4 children. The groups were balanced for age, sex, oppositional defiant disorder, and ethnicity | Trained observers, blind to treatment and diagnosis, observed the study children and classmates as a primary outcome | Strong quality (score 23/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described in companion methodological article presented by Klein et al. (2004). Insufficient data to assess sample size. Blinding for one of the primary outcomes was reported. Randomization not reported in detail. No estimates of variance reported. |
|
| ||||||
| Choi and Lee [ | Child training | Waitlist control | II | Block randomization scheme with blocks of 5 children. No evidence of stratification | No blinding of participants or personnel reported. All instruments were either parent- or child-report measures | Good quality score (18/28). Reliable use of peers. Sampling strategy appropriate with but only subject age, gender and school grade described. Blinding not reported for outcome measurement. Insufficient data to assess sample size. Estimates of variance provided for time points of interest, but not around the difference. |
|
| ||||||
| Frankel et al. [ | Child and parent training with medication | Waitlist control with medication | III | No randomization evident | No blinding of participants or personnel reported | Good quality (score 18/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Insufficient data to assess sample size. Blinding and randomization not reported. Authors reported the treatment and waitlist groups differed significantly in mean socioeconomic status however did not correlate with any outcome variable. Authors reported ADHD children were prescribed medication by their own private physicians and dosage was not verified by the present authors thus possibly affecting the results. |
|
| ||||||
| Guli et al. [ | Child training | Clinical control | III | No randomization evident | No blinding of participants or personnel reported | Good quality (score 20/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Insufficient data to assess sample size. Blinding and randomization not reported. Estimates of variance provided. Results reported in sufficient detail with supporting conclusions. Authors reported some children in the treatment and control group were taking prescription medication thus possibly affecting the results. |
|
| ||||||
| Haas et al. [ | Child training | Child training for no diagnosis control | III | No randomization evident | Counsellors who rated children's behaviour were naïve to the conduct problems and callous/unemotional traits status of each child | Good quality (score 20/28). Reliable use of peers. Sampling strategy not described. Subject characteristics sufficiently described. Blinding reported for one of the primary outcomes. Randomization not reported. Authors reported a relatively small sample with limited power to detect trends. As the sample only included children with high levels of CP and ADHD the data can only be safely generalised to children with high levels of CP and ADHD. Treatment outcomes may have been affected by medicated and unmedicated behaviour as some children were on medication for some (but not all) days therefore this may have affected results. |
|
| ||||||
| Hannesdottir et al. [ | Child training | Waitlist control | III | Randomization procedure not described | No blinding of participants or personnel reported | Good quality score (18/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Randomization was reported, but procedure not described. Blinding not reported. Insufficient information to calculate sample size. No estimates of variance around differences reported. |
|
| ||||||
| Hantson et al. [ | Child and parent training | Treatment as usual control | III | No randomization evident | No blinding of participants or personnel reported | Good quality (score 19/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described, however comorbidities were not reported. Blinding and randomization not reported. Relatively small sample size. No estimates of variance reported. |
|
| ||||||
| Huang et al. [ | Child and parent training | Community care control | II | No randomization evident | No blinding of participants or personnel reported | Good quality score (17/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Control group consisted of families interested in the program but unable to attend at specific appointment times, thus not truly randomized. No blinding reported. Insufficient information to calculate sample size. No estimates of variance around differences reported. Authors recognise that participants with good medication compliance had better outcomes on some measures, but did not control for medication compliance in all analyses. |
|
| ||||||
| Jensen et al. [ | Child, parent, and school-based training with medication | Community care control | II | Randomization was done centrally and stratified by site in blocks of 16 (4 to each group). Sealed, ordered envelopes were sent to sites for successive entries. Treatment assignment was concealed until the family confirmed agreement to accept randomization | No blinding of personnel reported | Good quality (score 21/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding was reported however it is not clear who was blinded. Randomization not described in detail. Appropriate samp |
|
| ||||||
| Kolko et al. [ | Child training | Child socialisation group | III | No randomization evident | Second trained research assistant unaware of child's group assignment recorded in vivo behavioural observations. Interrater agreement of behavioural role-play test were assessed by comparing ratings assigned by a trained research assistant unaware of group assignment | Good quality (score 18/28). Reliable use of peers. Sampling strategy may have introduced bias. Subject characteristics sufficiently described. Blinding was adequately reported for some of the raters however not all. Randomization was not reported. No estimates of variance reported. Appropriate sample size. |
|
| ||||||
| Mikami et al. [ | Child training for ADHD children | Child training for TD children | II | Randomly assigned via a computer-generated sequence either to a classroom in the MOSAIC treatment condition in Session 1 and a different classroom in the COMET treatment condition in Session 2 or vice versa. Assignment was stratified by child age and sex | Trained research assistants unaware of treatment group administered all primary outcome measures | Strong quality (score 25/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding was adequately reported for all outcome measures. Randomization was adequately reported. Estimates of variance provided. Authors reported a small sample size which limits the confidence for moderation results. |
|
| ||||||
| The MTA Cooperative Group [ | Child, parent, and school-based training with medication | Community care control | II | Randomization was done centrally and stratified by site in blocks of 16 (4 to each group). Sealed, ordered envelopes were sent to sites for successive entries. Treatment assignment was concealed until the family confirmed agreement to accept randomization | The open parent, teacher, and child ratings for 5 out of 6 outcomes were augmented by blinded ratings of school-based ADHD and oppositional/aggressive symptoms. Raters blind to treatment condition performed standardized laboratory tasks to assess parent-child interactions | Strong quality (score 24/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding was adequately reported. Randomization not reported in detail. Appropriate sample size based on power analyses. Explicit use of manualised, evidence-based treatments and comprehensive range of outcome assessments. Variance estimates reported inappropriately as study provided variance around the parameters of interest however not around the difference. |
|
| ||||||
| MTA Cooperative Group [ | Child, parent, and school-based training with medication | Community care control | II | Randomization was done centrally and stratified by site in blocks of 16 (4 to each group). Sealed, ordered envelopes were sent to sites for successive entries. Treatment assignment was concealed until the family confirmed agreement to accept randomization | No blinding of personnel reported | Good quality (score 21/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding not reported. Randomization not described in detail. Appropriate samp |
|
| ||||||
| Pfiffner et al. [ | Child and parent training with teacher consultation | Waitlist control or treatment as usual | II | Randomization was stratified by sex (when two children of the same sex were identified, one was randomly assigned to CLAS program and one to the control group). Investigators required at least two participants of the same sex in the treatment group | Interviewers and raters who were blind to child's group assignment administered the Test of Life Skill Knowledge outcome measure | Good quality (score 22/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding was adequately reported. Randomization was not reported in detail. No estimates of variance reported. Appropriate sample size. Participant use of medication was a confounding variable however unlikely to have seriously distorted results. |
|
| ||||||
| Shechtman and Katz [ | Child training for ADHD children | Waitlist control | II | The group was randomly divided (by alphabetical order) into an experimental and a waitlist control group (to be treated the next year) | No blinding of participants or personnel reported | Strong quality (score 24/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding not reported. Randomization was adequately reported. Estimates of variance provided. Appropriate sample size. Participant use of medication was not reported therefore may be confounding. |
|
| ||||||
| Storebø et al. [ | Child and parent training with standard treatment | Standard treatment alone | II | The Copenhagen Trial Unit conducted central randomization with computer-generated, permuted randomization sequences in blocks of four with an allocation ratio of 1 : 1 stratified for sex and comorbidity | The interventions given were not “blind” to participants, parents, treating physicians, or personnel. However, the outcome assessors (teachers) were kept blinded of the allocated intervention. Blinded data were then handed over for data entry and statistical analyses | Strong quality (score 26/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Blinding was adequately reported for all outcome measures. Blinding was not apparent for participants. Randomization was reported in detail. Estimates of variance provided. Sample size calculation completed with an appropriate sample size collected. |
|
| ||||||
| Waxmonsky et al. [ | Child and parent training with school-based daily report card and medication | Medication alone | II | One-half of the subjects were randomly assigned to receive atomoxetine + BT and the remaining subjects randomly assigned to receive atomoxetine alone | The second (reliability) observer for the behaviour therapy arm was blinded to group assignment | Good quality (score 22/28). Reliable use of peers. Sampling strategy appropriate with subject characteristics sufficiently described. Primary investigators were not blinded. Randomization was not reported in detail. Variance estimates reported inappropriately as study provided variance around the parameters of interest however not around the difference. Sample size was calculated for the primary outcome measure however not the secondary measures therefore sample may not have had sufficient subjects to detect group differences for secondary measures. |
Notes. NHMRC level II = RCTs; level III = quasi-experimental designs without random allocation; ADHD = Attention-Deficit Hyperactivity Disorder; CP = conduct problems; MOSAIC = Making Socially Accepting Inclusive Classrooms; COMET = contingency management training; and CLAS = Child Life and Attention Skills program.
Figure 2Publication bias funnel plot.
Figure 3Within intervention group pre-post meta-analysis. Notes. Hedges' g interpreted as per Cohen's d conventions: ≤0.2 = negligible difference, 0.2–0.49 = small, 0.5–0.79 = moderate, and ≥ 0.8 = large.
Subgroup analysis comparing intervention groups of included studies.
| Subgroups | Hedges' |
|
|
|---|---|---|---|
|
| 0.595 | 9.085 | <0.001 |
| No parent involvement ( | 0.606 | 4.606 | <0.001 |
| Parent involvement ( | 0.577 | 7.833 | <0.001 |
|
| 0.629 | 11.344 | <0.001 |
| RCT ( | 0.643 | 11.025 | <0.001 |
| Quasi-experimental ( | 0.496 | 2.784 | 0.001 |
|
| 0.609 | 5.696 | <0.001 |
| Good ( | 0.576 | 7.206 | <0.001 |
| Strong ( | 0.588 | 3.712 | <0.001 |
|
| 0.608 | 11.176 | <0.001 |
| Blinded ( | 0.622 | 10.187 | <0.001 |
| No blinding ( | 0.556 | 4.623 | <0.001 |
|
| 0.594 | 9.999 | <0.001 |
| Parent + teacher ( | 0.832 | 6.786 | <0.001 |
| Parent ( | 0.496 | 4.689 | <0.001 |
| Self ( | 0.517 | 5.023 | <0.001 |
| Teacher ( | 0.547 | 5.023 | <0.001 |
Notes. Significant.
Metaregression results.
| Set | Covariate | 95% lower | 95% upper |
| 2-sided |
|---|---|---|---|---|---|
| Intercept | −0.0527 | 2.0452 | 1.86 | 0.0627 | |
| Blinding: no blinding | −0.5548 | 0.158 | −1.09 | 0.2752 | |
| Parent Component: parent involvement | −0.5257 | 0.4463 | −0.16 | 0.8729 | |
| Methodological quality: strong quality | −0.5003 | 0.5989 | 0.18 | 0.8603 | |
| Study design: RCT | −0.5616 | 0.6237 | 0.10 | 0.9182 | |
|
| Rater: parent-rated | −0.9472 | −0.0091 | −2.00 | 0.0457 |
|
| Rater: self-rated | −0.959 | 0.4601 | −0.69 | 0.4908 |
|
| Rater: teacher- rated | −1.0655 | 0.1701 | −1.42 | 0.1555 |
Notes. Significant.