| Literature DB >> 34401386 |
Liang Ma1, Cong Huang2,3, Rimeng Tao1, Zeshi Cui4, Philip Schluter5.
Abstract
OBJECTIVE: This meta-analysis examines the effect of online guided self-help interventions for depressive symptoms among college students.Entities:
Keywords: College students; Depressive symptoms; Guided; Internet; Meta-analysis
Year: 2021 PMID: 34401386 PMCID: PMC8350612 DOI: 10.1016/j.invent.2021.100427
Source DB: PubMed Journal: Internet Interv ISSN: 2214-7829
Fig. 1PRISMA flowchart.
Description and characteristics of included studies.
| Author | Student sample ( | Recruit | Setting | Age (mean) | Female% | Sample type | Online intervention ( | Control ( | Contact level | Follow-up (wk) | Incentive | Group format | Symptom measure | Country |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Students with mild to moderate levels of anxiety, depression or stress: DASS ≥ 8, 10, 15 ( | Online | Campus | 23.6 | 89 | S | CBT ( | WL ( | Trained students ( | 6, 24 | No | – | DASS | CAN | |
| Students with elevated scores on the Kessler Psychological Distress Scale: K10 < 30 ( | On-site | Campus | 19.7 | 77 | S | Online CBT: The MoodGYM intervention ( | AO ( | Researcher ( | 3 | Yes | – | DASS | AUS | |
| General ( | Online | Campus | 25 | 79 | U | Acceptance-based behavioral intervention ( | WL ( | Doctoral candidate in clinical psychology ( | 4 | Yes | – | DASS | USA | |
| Students with mildly and moderately depressed undergraduates: CES-D ≥ 10 and <25 ( | Online | Campus | NS | 83 | I | iCBT (Moodgym) ( | AO ( | Research team member ( | 5, 7 | Yes | – | CES-D | USA | |
| Students with elevated levels of stress: PSS-4 ≥ 8 ( | Online | Campus | 24.1 | 75 | S | iCBT for stress (StudiCare Stress) ( | WL ( | Trained students ( | 7, 12 | No | – | BDI | GER | |
| First-year students ( | On-site | Campus | 18.4 | 54 | U | ACT ( | WL ( | Regular contact ( | 3, 6 | Yes | – | DASS | USA | |
| General ( | Online | Campus | 21 | 66 | U | ACT ( | WL ( | Research assistants ( | 4 | Yes | – | CCAPS-D | USA | |
| Students with receiving mental health counseling ( | On-site | Campus | 25 | 68 | S | PA ( | UC ( | Counselor ( | 10 | No | – | BDI | USA | |
| General ( | Online | Campus | 20.5 | 67 | U | CBT programs: “Insomnia Relief” ( | WL ( | Standardized emails ( | 6 | Yes | – | BDI | UK | |
| Students with self-identified as experiencing symptoms of anxiety or depression ( | Online | Campus | 27.9 | 64 | S | CBT ( | WL ( | Psychologist ( | 6, 12 | Yes | – | PHQ | AUS | |
| Students with self-reporting as experiencing some form of psychological distress ( | Online | Campus | 24 | 85 | S | ACT ( | WL ( | Trained psychology students ( | 7, 48 | No | – | BDI | FIN | |
| Students with self-reported GAD symptoms: GAD-7 ≥ 10 ( | Online | Campus | 23.8 | 77 | S | CBT ( | WL ( | Psychologists ( | 6 | No | – | BDI | IRL | |
| First-year students with low to moderate levels of depression and/or anxiety (38) | On-site | Campus | 19.5 | 66 | S | iCBT (Moodgym) ( | AO ( | Psychologists ( | 3 | Yes | – | DASS | AUS | |
| General ( | Online | Campus | 26.9 | 67.8 | U | ACT ( | WL ( | Standardized emails ( | 4 | No | – | DASS | AUS | |
| Undergraduates ( | Online | Campus | 23.1 | 76 | U | Mindfulness virtual community ( | WL ( | Moderators ( | 8 | Yes | LVC | PHQ | CAN | |
| Students with elevated repetitive thoughts: PSWQ ≥ 50; RRS ≥ 40 ( | Online | Public | 20.4 | 83 | S | CBT ( | UC ( | Clinician ( | 12 | No | – | PHQ | UK | |
| Students with mild to moderately severe depressive symptoms: PHQ ≥ 10 and <19 (214) | Online | Campus | 22.2 | 71 | I | CBT ( | WL ( | Postgraduate student in clinical psychology ( | 7, 12 | No | – | PHQ | CO | |
| Undergraduates ( | Online | Campus | 24.8 | 75 | U | Full mindfulness virtual community ( | WL ( | Moderators ( | 8 | Yes | LVC | PHQ | CAN | |
| Undergraduates ( | Online | Campus | 22.6 | 79 | U | Mindfulness virtual community ( | WL ( | Moderators ( | 8 | Yes | LVC | PHQ | CAN |
Note. U = universal; S = selective; I = indicated; M = moderate; H = high; WL = wait-list; UC = usual-care; AO = assessment-only; LVC = live video conference. NS = not specified; BDI = Beck Depression Inventory; DASS = Depression, Anxiety, and Stress Scales; PHQ = Patient Health Questionnaire; CES-D = Centre for Epidemiologic Studies-Depression; CCAPS-D = Counseling Center Assessment of Psychological Symptoms-Depression.
Risk of bias assessment.
| Author | The randomization process | Missing outcome data | Measurement of the outcome | Selection of the reported result | Overall |
|---|---|---|---|---|---|
| + | + | + | ~ | Moderate | |
| – | ~ | + | ~ | High | |
| ~ | – | + | ~ | High | |
| – | ~ | + | ~ | High | |
| + | + | + | ~ | Moderate | |
| – | + | + | ~ | High | |
| ~ | + | + | ~ | Moderate | |
| – | + | + | ~ | High | |
| ~ | + | + | ~ | Moderate | |
| ~ | + | ~ | ~ | Moderate | |
| ~ | + | – | + | High | |
| + | + | + | + | Low | |
| – | + | ~ | ~ | High | |
| ~ | + | + | ~ | Moderate | |
| + | + | + | ~ | Moderate | |
| + | + | ~ | + | Moderate | |
| + | – | + | ~ | High | |
| + | + | + | ~ | Moderate | |
| + | + | + | ~ | Moderate |
Note. + = lower risk of bias; − = higher risk of bias; ~ = some concern.
Fig. 2Forest plot for the meta-analysis of online guided self-help interventions on depressive symptoms.
Subgroup analyses by hypothesized variables.
| Subgroup | No. | Effect sizes | ||||
|---|---|---|---|---|---|---|
| Comparisons | Intervention condition | Control condition | Hedge's | Heterogeneity | ||
| Type of sample | 0.26 | |||||
| Universal | 10 | 1077 | 967 | 0.27 (0.18, 0.36) | I2 = 0, | |
| Selective | 11 | 393 | 358 | 0.47 (0.30, 0.64) | I2 = 16.9%, | |
| Length of intervention | 0.46 | |||||
| Brief | 8 | 795 | 745 | 0.29 (0.16, 0.42) | I2 = 6.1%, | |
| Moderate | 9 | 375 | 302 | 0.52 (0.37, 0.68) | I2 = 0, | |
| Long | 6 | 343 | 300 | 0.25 (0.09, 0.41) | I2 = 0, | |
| Level of contact | 0.70 | |||||
| High | 5 | 200 | 177 | 0.42 (0.10, 0.74) | I2 = 43.8%, | |
| Moderate | 15 | 626 | 557 | 0.40 (0.29, 0.52) | I2 = 0, | |
| Low | 3 | 687 | 613 | 0.24 (0.13, 0.34) | I2 = 0, | |
| Use of incentive | 0.92 | |||||
| Yes | 16 | 598 | 469 | 0.36 (0.23, 0.48) | I2 = 0, | |
| No | 7 | 915 | 878 | 0.39 (0.21, 0.57) | I2 = 52.0%, | |
| Intervention content | 0.99 | |||||
| CBT | 12 | 444 | 356 | 0.42 (0.27, 0.57) | I2 = 6.6%, | |
| Third-wave | 10 | 1043 | 966 | 0.32 (0.21, 0.44) | I2 = 15.2%, | |
| PRISMA checklist | |||
|---|---|---|---|
| Section/topic | # | Checklist item | Reported on page # |
| Title | |||
| Title | 1 | Identify the report as a systematic review, meta-analysis, or both. | 2 |
| Abstract | |||
| Structured summary | 2 | Provide a structured summary including, as applicable: background; objectives; data sources; study eligibility criteria, participants, and interventions; study appraisal and synthesis methods; results; limitations; conclusions and implications of key findings; systematic review registration number. | 1 |
| Introduction | |||
| Rationale | 3 | Describe the rationale for the review in the context of what is already known. | 2–6 |
| Objectives | 4 | Provide an explicit statement of questions being addressed with reference to participants, interventions, comparisons, outcomes, and study design (PICOS). | 6–7 |
| Methods | |||
| Protocol and registration | 5 | Indicate if a review protocol exists, if and where it can be accessed (e.g., Web address), and, if available, provide registration information including registration number. | N/A |
| Eligibility criteria | 6 | Specify study characteristics (e.g., PICOS, length of follow-up) and report characteristics (e.g., years considered, language, publication status) used as criteria for eligibility, giving rationale. | 7 |
| Information sources | 7 | Describe all information sources (e.g., databases with dates of coverage, contact with study authors to identify additional studies) in the search and date last searched. | 7 |
| Search | 8 | Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated. | 7, 25 |
| Study selection | 9 | State the process for selecting studies (i.e., screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis). | 8 |
| Data collection process | 10 | Describe method of data extraction from reports (e.g., piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators. | 8 |
| Data items | 11 | List and define all variables for which data were sought (e.g., PICOS, funding sources) and any assumptions and simplifications made. | 8–9 |
| Risk of bias in individual studies | 12 | Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level), and how this information is to be used in any data synthesis. | 9–10 |
| Summary measures | 13 | State the principal summary measures (e.g., risk ratio, difference in means). | 10 |
| Synthesis of results | 14 | Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e.g., I2) for each meta-analysis. | 11–12 |
| Risk of bias across studies | 15 | Specify any assessment of risk of bias that may affect the cumulative evidence (e.g., publication bias, selective reporting within studies). | 11 |
| Additional analyses | 16 | Describe methods of additional analyses (e.g., sensitivity or subgroup analyses, meta-regression), if done, indicating which were pre-specified. | 11–12 |
| Results | |||
| Study selection | 17 | Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram. | 12 |
| Study characteristics | 18 | For each study, present characteristics for which data were extracted (e.g., study size, PICOS, follow-up period) and provide the citations. | 37–38 |
| Risk of bias within studies | 19 | Present data on risk of bias of each study and, if available, any outcome level assessment (see item 12). | 13, 39 |
| Results of individual studies | 20 | For all outcomes considered (benefits or harms), present, for each study: (a) simple summary data for each intervention group (b) effect estimates and confidence intervals, ideally with a forest plot. | |
| Synthesis of results | 21 | Present results of each meta-analysis done, including confidence intervals and measures of consistency. | 14–16 |
| Risk of bias across studies | 22 | Present results of any assessment of risk of bias across studies (see item 15). | 14–16 |
| Additional analysis | 23 | Give results of additional analyses, if done (e.g., sensitivity or subgroup analyses, meta-regression [see item 16]). | 14–17 |
| Discussion | |||
| Summary of evidence | 24 | Summarize the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (e.g., healthcare providers, users, and policy makers). | 17–19 |
| Limitations | 25 | Discuss limitations at study and outcome level (e.g., risk of bias), and at review-level (e.g., incomplete retrieval of identified research, reporting bias). | 20 |
| Conclusions | 26 | Provide a general interpretation of the results in the context of other evidence, and implications for future research. | 21 |
| Funding | |||
| Funding | 27 | Describe sources of funding for the systematic review and other support (e.g., supply of data); role of funders for the systematic review. | N/A |