| Literature DB >> 35548259 |
Karen Hurtubise1, Astrid Brousselle1,2, Chantal Camden1,3.
Abstract
Intensive interdisciplinary pain treatment (IIPT) involves multiple stakeholders. Mapping the program components to its anticipated outcomes (ie, its theory) can be difficult and requires stakeholder engagement. Evidence is lacking, however, on how best to engage them. Logic analysis, a theory-based evaluation, that tests the coherence of a program theory using scientific evidence and experiential knowledge may hold some promise. Its use is rare in pediatric pain interventions, and few methodological details are available. This article provides a description of a collaborative logic analysis methodology used to test the theoretical plausibility of an IIPT designed for youth with pain-related disability. A 3-step direct logic analysis process was used. A 13-member expert panel, composed of clinicians, teachers, managers, youth with pain-related disability, and their parents, were engaged in each step. First, a logic model was constructed through document analysis, expert panel surveys, and focus-group discussions. Then, a scoping review, focused on pediatric self-management, building self-efficacy, and fostering participation, helped create a conceptual framework. An examination of the logic model against the conceptual framework by the expert panel followed, and recommendations were formulated. Overall, the collaborative logic analysis process helped raiseawareness of clinicians' assumptions about the program causal mechanisms, identified program components most valued by youth and their parents, recognized the program features supported by scientific and experiential knowledge, detected gaps, and highlighted emerging trends. In addition to providing a consumer-focused program evaluation option, collaborative logic analysis methodology holds promise as a strategy to engage stakeholders and to translate pediatric pain rehabilitation evaluation research knowledge to key stakeholders.Entities:
Keywords: interdisciplinary pain rehabilitation program; intervention theory; logic analysis; logic model; pediatric chronic pain; theory‐based evaluation
Year: 2020 PMID: 35548259 PMCID: PMC8975192 DOI: 10.1002/pne2.12018
Source DB: PubMed Journal: Paediatr Neonatal Pain ISSN: 2637-3807
FIGURE 1Association between the logic analysis steps and results
Summary of logic analysis steps, processes, and procedures
| Logic model methodology | ||
|---|---|---|
| Steps | Process | Procedures |
| 1. Logic model construction: Create a representation of the intervention's program theory and the links between resources, activities processes, and anticipated outcome, using diverse data sources (Brousselle & Champagne, 2011) | Review of all historical program document | Deductive analysis using data extraction form based on logic model components by research team |
| Expert panel electronic survey | Deductive analysis using data extraction form based on logic model components by research team | |
| Draft logic model created by research team using data gathered in documents and surveys | ||
|
Group discussion
Validate the primary program objective Review and modify anticipated outcomes (short, medium, and long term) Review and modify resources, activities, and processes Review and modify reach and important contextual factors Establish perceived links between components and anticipated outcomes Achieve agreement on final logic model |
Updates of the draft logic model after each meeting by research team. Each subsequent draft returned to expert panel members for further discussion and detailing until agreement achieved. | |
| Agreement reached by the expert panel members on the logic model representation | ||
| 2. Conceptual framework development: Identify and examine the evidence, and document the mechanisms similar to those attributed to the intervention, providing a representative synthesis of the most recent knowledge in the most relevant and meaningful fields of research (Brousselle & Champagne, 2011) |
Scoping review framework (Levac et al., 2010) Identify research question Identifying relevant studies Study selection Charting the data Collating, summarizing, and reporting the results Consultation |
Expert panel discussion conducted to identify and achieve agreement on the research question and the study inclusion and exclusion criteria. Studies identified by the research team. Final selection presented to expert panel for approval. Data extracted and deductive analysis completed by research team using a form based on the logic model components and the primary program objective. Draft conceptual framework created by research team and presented to the expert panel for discussion and validation. Expert panel consulted throughout the scoping review process and assisted in the re‐interpretation of the findings in the context of IIPT |
| Agreement reached by the expert panel on the interpretation of the conceptual framework | ||
| 3. Evaluating the program theory: Review the logic model in light of the evidence contained in the conceptual framework, highlighting the intervention's strengths, weaknesses, and recommendations for improvement (Brousselle & Champagne, 2011) | The logic model was compared to the evidence contained in the conceptual framework for convergence (ie, IIPT strengths) and divergence (ie, IIPT weaknesses and gaps) |
A list of strengths, weaknesses, and gaps of the IIPT was identified by the research team, IIPT improvement recommendations formulated, and presented to the expert panel for discussion. Following discussion, only improvement recommendations upon which consensus among the expert panel members was achieved were presented to the hospital leadership team. |
Document and survey analysis
| Data sources | Document title (y) | Program logic model components | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Program goals | Program objectives | Reach | Eligibility | Program resources | Program activities | Program outcomes | Program context | ||
| Program documents (n = 15) | Initial Program Description (2013) | Not consistent | Absent | Not consistent | Absent | Not consistent | Absent | Not consistent | Absent |
| Program Curricula (2015‐2018) | Absent | Absent | Absent | Absent | Not consistent | Not consistent | Absent | Absent | |
| Program Goals and Objectives (2016) | Not consistent | Not consistent | Absent | Absent | Not complete | Not complete | Absent | Absent | |
| Program Implementation Evaluation (2016) | Not consistent | Not consistent | Not complete | Absent | Not complete | Not consistent | Not consistent | Absent | |
| Program Referral Guide (2017) | Absent | Absent | Absent | Complete for youth only | Not complete | Absent | Absent | Absent | |
| Program Information for Patients and Families (2016) | Not consistent | Not consistent | Not complete | Absent | Not consistent | Not complete | Absent | Absent | |
| General Information for Youth and Families (2016) | Not consistent | Absent | Not complete | Complete for youth & families | Not consistent | Not complete | Absent | Absent | |
| Overall judgment after document analysis | Not consistent | Not consistent | Complete for youth & families | Not consistent or complete | Not consistent or complete | Not consistent | Absent | ||
| Stakeholder surveys (n = 13) | Survey questions | What are the goals & objectives of the IIPT? | Who should the program target? | No further information required | Who and what help accomplish the objective(s) of the program? | What are the effects of the program? | Context Analysis | ||
| Overall judgment after survey analysis | Still not consistent | Complete for youth & families | Not consistent | Priority setting | Not consistent | ||||
| Stakeholder focus groups (n = 6) | Focus group guiding questions | Is each component representative of the current program? | |||||||
| Overall judgment after focus groups | Complete | Expanded to include school personnel | Causal mechanisms clarified | Validated | Complete | ||||
Summary of studies retained for conceptual framework development
| Authors & publication year | Country | Study design | Study aim | Population characteristics | Feature of included studies | Key findings |
|---|---|---|---|---|---|---|
| Self‐management interventions (SMI) | ||||||
| Stinson et al (2008) | Canada | Systematic Review | To critically appraise the evidence on effectiveness of Internet‐based SMI on health outcomes in youth with chronic conditions. | Children and adolescents (6‐18 y). Asthma, recurrent pain, encopresis, traumatic brain injury, obesity. | 7 randomized control trials, 1 pilot randomized control trail, and 1 quasi‐experimental study. | Internet‐based SMI have demonstrated some evidence improving symptoms and disease self‐management yet are inconclusive in whether as effective as in‐person individualized or group interventions. |
| Lindsay et al (2011) | Canada | Integrative Review | To synthesize findings from empirical studies examining influential factors of adolescents’ self‐management of chronic illness. |
Adolescents and young adults (12‐20 y). Diabetes, asthma, spina bifida, inflammatory bowel disease, juvenile idiopathic arthritis. | 34 studies, 16 qualitative, 14 quantitative, and 4 mixed‐methods designs. | Psychosocial factors (eg, self‐efficacy), parent involvement, and knowledge about illness are important facilitators. Youth self‐management skills should be assessed, along with their social and developmental context to identify supports. |
| Lindsay et al (2014) | Canada | Systematic Review |
To systematically assess the effectiveness of SMI for school‐aged children with physical disabilities. |
Adolescents and young adults (13‐24 y) Children and adolescents (2‐18 y) Spina bifida, juvenile rheumatoid arthritis, juvenile idiopathic arthritis | 2 randomized control trials; 4 before and after designs. |
Intervention components should include knowledge about condition, medication management, psychosocial factors (eg, self‐efficacy). Parental involvement can be a barrier to self‐management and should be carefully assessed. |
| Sattoe et al (2015) | Netherlands | Systematic Review | To provide a systematic overview of the SMI for young people with chronic conditions. |
Children (7‐11 y) and adolescents (12‐18 y) Asthma, diabetes, cancer, chronic fatigue, chronic pain, chronic respiratory conditions, inflammatory bowel disease, juvenile fibromyalgia, juvenile idiopathic arthritis, migraine, physical disabilities, sickle cell. | 45 randomized control trials, 29 cohort studies, 3 cross‐sectional studies, 3 qualitative, 5 mixed‐methods, 1 case study, 26 pilot evaluations. | Role and emotional management should be included in SMI, along with medical management. Parents can either facilitate or hinder youth self‐management. Experiential learning, peer learning for others, and mastery experience strategies are appropriate pediatric SMI. Developmental factors need to be considered. |
| Bal et al (2016) | Netherlands | Systematic Review |
To systematically explore the effectiveness and effective components of SMI. |
Children to young adults (7‐25 y) Asthma, diabetes, cystic fibrosis, cancer, HIV, sickle cell, spina bifida, hemophilia, juvenile fibromyalgia. | 42 randomized control trials. | SMI should focus on medical, emotional, and role management in the context of youth's daily lives. Peer support stimulates self‐efficacy. Online peer support could improve self‐efficacy, problem‐solving, and coping behaviors. |
| Lindsay, Kolne, Cagliostro (2018) | Canada | Systematic Review | Synthesis and review literature on the impact of electronic mentoring for children with disabilities | Children to young adults (12‐26 y). Rheumatic disease, juvenile arthritis, cerebral palsy, spina bifida, muscular dystrophy, pediatric transplant, visual impairments, chronic pain. | 3 RCTs, 7 surveys, 1 case study, 1 feasibility study. | Electronic mentoring is effective for children and youth with disabilities in improving career decision‐making, self‐determination, self‐management, self‐confidence, self‐advocacy, social skills, attitude toward disability, and coping with daily life. |
| Self‐efficacy | ||||||
| Cramm et al (2013) | Netherlands | Cross‐sectional study | To investigate the influence on general self‐efficacy perceived by adolescents with chronic conditions and parents on quality of life. |
Adolescents, and young adults (12‐25 y) and their parents Diabetes, juvenile rheumatoid arthritis, cystic fibrosis, urology conditions and neuromuscular disorders. | Not applicable. | Interventions aimed at improving general self‐efficacy should include activities that seek to enhance confidence and the ability to deal effectively with difficult and unexpected events. |
| Johnson et al (2015) | United States (US) | Cross‐sectional study | To determine the preferred methods for health information among youths with chronic conditions and their relationship to healthcare transition readiness, self‐efficacy, and medication adherence. |
Children and adolescents (6‐16 y) Diabetes, musculoskeletal conditions, cerebral palsy, heart disease, neurological and gastrointestinal condition. | Not applicable. |
Youth with chronic conditions receive their health information from physicians/nurses, parents/family, and the Internet. A range of health information should be considered to include those that deliver it directly to the patient, the family/parent, including the Internet, allowing youth to select their preferred method. |
| Molter & Abrahamson (2015) | United States | Literature Review | To investigate the relationship among self‐efficacy, transition, and health outcomes. | Children, adolescents, and adults (6‐55 y). Sickle cell. | 20 studies of various unspecified designs. |
Knowledge of condition, body awareness, and spirituality are factors that affect self‐efficacy. Journaling, self‐awareness, scripture reading, and prayer activities can increase feelings of self‐efficacy. Experiences of acting independently and developing patient‐health provider partnerships are important. Education, counseling, and advocacy interventions to the broader public could be used to decrease stigmatization. |
| Kalapurakkel et al (2014) | United States | Cross‐sectional study | To examine pain self‐efficacy and pain acceptance in relation to functioning in pediatric headache patients. | Children and adolescents (8‐17 y); Headache. | Not applicable. | Higher levels of self‐efficacy are associated with improved school functioning, fewer depressive symptoms, and lower disability levels, higher self‐esteem and fewer somatic symptoms. |
| Tomlinson et al (2017) | Canada | Literature Commentary | To examine the resilience mechanism of pain self‐efficacy. | Children and adolescents. | Not specified. |
Exposure to and mastery of feared activities reinforces self‐efficacy. Generalizing prior successes that highlight mastery and increase confidence can enhance pain self‐efficacy. Mindfulness and biofeedback are also helpful modalities. The identification of valued goals and utilizing graded exposure techniques to previously avoided activities promote self‐efficacy. |
| Participation | ||||||
| Pinquart & Teubert (2011) | Germany | Meta‐analysis | To compare the levels of academic, physical, and social functioning of children and adolescents with chronic physical diseases with those of healthy peers. |
Children and adolescents (under the age of 18 y) Arthritis, asthma, cancer, chronic fatigue, cystic fibrosis, cerebral palsy, inflammatory bowel disease, headaches, diabetes, hemophilia, epilepsy, sickle cell, spina bifida. | 954 studies designed not specified. |
Sports and leisure activity counseling should be available to guide these youth. Teachers and coaches should promote participation in sports to improve physical functioning. School functioning can be improved with school accommodations. Group social skills training provides youth with strategies to deal with teasing and bullying. |
| Anaby et al (2015) | Canada | Scoping Review |
To identify and analyze research evidence regarding the effect of the environment on community participation of children with disabilities. |
Children, adolescents and young adults (5‐21 y). Cerebral palsy, physical disabilities (with restricted mobility due to neurological or musculoskeletal disorders), acquired brain injury, autism spectrum disorder, Down syndrome. | 31 studies; 17 qualitative, 10 qualitative, review 3, 1 mixed‐method design. |
Negative attitudes within the communities can be a barrier to participation. Parental involvement and advocacy can influence on social functioning, participation, and friendship development. Peers, teacher, and service provider support fostering participation. Parental over‐protectiveness and stress can limit participation. Parental education about recreation activities and advocacy supports participation. |
| Adair et al (2015) | Australia | Systematic review | To critically appraise studies aimed at improving participation outcomes of children with disabilities. | Children and adolescents with disabilities (5‐18 y) such as cerebral palsy, developmental coordination disorder, autism spectrum disorder, arthrogryposis, intellectual disabilities. | 7 randomized control or nonrandomized trials |
Tailored programs using both individual‐ and group‐based approaches can enhance participation. Coaching approaches focused on mutually agreed upon goals are effective. Practice of desired behaviors in a social context is proven useful. |
| Forgeron et al (2018) | Canada | Systematic Review | To identify the psychosocial interventions found to be most promising in their effectiveness in improving social functioning outcomes of children and adolescents with a wide range of chronic physical health conditions. | Children and adolescents (5‐18 y) with diabetes, epilepsy/seizures, cerebral palsy, spina bifida, inflammatory bowel disease, burn scaring, chronic respiratory condition. | 13 studies; 10 nonrandomized control trials, 3 randomized control trials. | Most improvements in social functioning stemmed from interventions that focused on a broad range of social skill development rather than solely on communication about condition with peers. Interventions that consisted of more than one session targeting social functioning were more promising. A paucity of evidence exists on effective interventions. |
| Jones et al (2018) | Canada | Narrative review | To review selected studies that have made an impact on the field of school functioning in children and adolescents with chronic pain. | Children and adolescents (8‐18 y) with chronic pain such as abdominal, myofascial, neuropathic, limb, back pain, headache. | 13 nonrandomized control trials. | Evidence suggests that psychological factors (depression and anxiety), social factors (peer relationships, perception of teachers support, parent protectiveness), physiological factors (sleep disturbance), and cognitive factors (self‐efficacy, memory, and attention deficits) may interact to influence school functioning. |
| Ideal context | ||||||
| Stahlschmidt et al (2016) | Germany | Review | To present an international perspective on the structure and components of pain rehabilitation programs worldwide. | 9 different programs from 4 different countries. | 15 descriptive or nonrandomized studies. | Specialized rehabilitation programs for disabling chronic pain conditions worldwide have similar admission criteria, structure, and therapeutic orientation. Differences in exclusion criteria impede program comparability. |
| Miró et al (2017) | Spain | Cross‐sectional study design using surveys | To identify the features’ current chronic pain programs and describe the feature required to achieve an ideal state. | 136 pediatric pain experts located in 12 different countries. | Not applicable. | Staff should be multidisciplinary, with research and formal specialty training available. A wide variety of treatment options should be offered and publicly funded. |
| Harrison et al (2019) | United States, Belgium, Stockholm | Review | To present an overview of rehabilitation interventions for children and adolescents with chronic pain and to inform clinicians on the innovative treatment delivery and patient outcomes. | Not applicable. | Systematic review, meta‐analyses, clinical trials with sample >20, clearly describing the intervention. | Patients who have been unsuccessful at outpatient treatment are targeted. Must include three or more disciplines housed within the same facility (eg, pain specialist, psychologist, and physical therapist) who work in an integrated manner to provide treatment. Patient must participate in exercise‐based therapy and psychological interventions. The aim is to improve function across domains. Variability exists in program structure, organization, frequency of treatment across disciplines, treatment model (inpatients vs. day‐hospital), and length of stay. |
Conceptual framework
| Logic model components | Self‐management interventions | Building self‐efficacy | Fostering participation |
|---|---|---|---|
| Program objectives | |||
| Program goals and objectives | Role, and emotional and medical self‐management relative to developmental expectations should be integrated within youth's daily life and relevant social contexts | ||
| Program reach and eligibility |
Parent involvement should be carefully assessed Education should extend beyond youth with chronic conditions and parents, to include peers and teachers | Education initiatives should target peers, classmates, teachers, and community leaders (eg, coaches) | |
| Program activities |
Psychoeducation, combining information and skills training, is the focus of self‐management interventions Parent education, parent‐to‐parent support, and using parent coaching approaches are effective in fostering independence in youth self‐management Experiential approaches, varying delivery methods (group, individualized, Internet‐based), peers learning opportunities, and skill mastery experiences should be provided Communication, assertiveness, and advocacy training are a need identified by youth to promote shared decision‐making with professionals Opportunities for youth to create their own patient‐professional relationships can be enriching Peer‐to‐peer learning and mentoring is an emerging model showing promise |
Activities that build independence, life, and leadership skills should be promoted Opportunities for youth to create their own patient‐professional relationships can be enriching Self‐awareness (eg, journaling), self‐directed learning (eg, web‐based resources), and spiritual program activities, using a variety of learning methods and mediums (eg, health professionals, parents, Internet‐based modules) should be included Biofeedback, self‐regulation, relaxation, mindfulness, cognitive‐behavioral therapy, value‐based goal identification nurture self‐efficacy Successful accomplishment of assigned tasks and generalization of prior successes, and graded exposure to fear‐eliciting activities are also beneficial |
Individualized and group‐based interventions are effective when combined Physical and leisure activity selection should be guided by mutually agreed upon participation goals and identified through coaching approaches Training parents and youth on how to advocate for social inclusion and how to adapt and modify the activity and environment are effective strategies to minimize participation barriers Sport and leisure activity counseling and social skills training should be available Coaching on how to communicate about the condition and the supports required may be beneficial for this population in peer and school settings More complex age‐specific in‐person sessions expanding social skills training to peer interactions, conflicts (eg, bullying), and intimate friendships may also be beneficial for older adolescents |
| Program outcomes |
Increased knowledge and skills in problem‐solving, decision‐making, and advocacy have been described Improvements in self‐efficacy, psychosocial well‐being, and family functioning, along with reduction in social isolation, school absenteeism and pain have been demonstrated Reduced family and parent burden, reducing healthcare utilization, and improving overall health outcomes and quality of life have also been reported |
Benefits to physical, emotional, and school functioning have been recognized Self‐efficacy has been identified as a key contributor to chronic disease self‐management, to promoting of long‐term behavior change, to improving the appropriateness of healthcare utilization practices, and to enhancing health quality of life | Participation improved academic performance, social interactions, mental and physical health, and helps develop life purpose and meaning |
| Creating the ideal context | |||
| Program resources |
Program should be publicly funded A variety of health disciplines with specific training and expertise in pediatric pain A clinical and research training role, along with a public education (eg, school personnel) and advocacy mandate should be fulfilled by the program Youth with variety of pain conditions, regardless of the type and origin, and their parents should be targeted | ||
FIGURE 2Expert panel agreed upon logic model