- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05587634
Virtual Peer Health Coaching for Adolescents With Disabilities
Virtual Peer Health Coaching as an Effective Intervention for Increasing Physical Activity in Adolescents With Physical Disability
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Physical activity is an often overlooked, yet incredibly powerful, tool for empowering adolescents with disabilities to take control of their own physical and psychosocial health. At least 60 minutes of daily physical activity (PA) is recommended for children and adolescents ages 6-17, yet the vast majority of young people with disabilities do not meet these goals. As a result, children and adolescents with disabilities are more likely than their non-disabled peers to experience the detrimental impact of sedentary lifestyles such as high rates of obesity/overweight - adverse health trends that continue into adulthood. Additionally, given that children and adolescents with disabilities remain systematically excluded from community and school-based sports and PA opportunities - a mainstay of social development and confidence-building in able-bodied youth - those with disabilities are more likely to experience social isolation and thus threats to well-being and quality of life.
In this context, prior research has focused on the role of peer health coaching (PHC) to enhance health self-management in individuals with disabilities, demonstrating efficacy in reducing rates of secondary conditions and improving self-efficacy and life satisfaction. PHCs simultaneously act as advisor, supporter, and role model, providing the "hook" that stimulates behavior change. Although the PHC model has also been used to promote participation in PA, studies have focused on adults primarily with spinal cord injury. While it is well known that engagement in PA in adolescence is correlated with similar behaviors in adulthood, no prior trials have explored the efficacy of PHCs in stimulating PA behavior in adolescents with childhood-onset disability.
To explore effective solutions that stimulate PA participation to promote equity and quality of life in adolescents with disabilities, this pilot study will target adolescents with cerebral palsy (CP) and spina bifida (SB), the 2 most common types of childhood-onset physical disability, with the following specific aims:
Primary Objective:
To evaluate the feasibility of conducting an efficacy trial of the first virtual PHC intervention aimed to increase PA participation in adolescents with CP and SB. This will include assessing the acceptability of the intervention to our key stakeholders - adolescents with disabilities and their families.
Secondary Objective:
To determine the responsiveness of selected outcome measures to the first virtual PHC intervention in adolescents with CP and SB. Outcomes will include the assessment of a) physical activity, b) psychosocial health, and c) quality of life.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
-
Charlestown, Massachusetts, United States, 02129
- Spaulding Rehabilitation Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adolescents ages 12-17 years
- Primary residence in cities and towns within greater Boston
- Presence of CP or SB resulting in mobility limitation
- CP - Gross Motor Function Classification System (GMFCS) level II and III
- SB - myelomeningocele, lipomyelomeningocele, or tethered cord syndromes with motor impairment
- Fluent in conversational English
- Able to utilize a personal cell phone for verbal and text message communications
- Intentions of engaging in PA
Exclusion Criteria:
- Presence of significant cognitive impairment - IQ below 55 as measured by Wechsler Intelligence Score for Children (WISC) or Wechsler Adult Intelligence Scale (WAIS), or those below a 3rd grade reading level
- Use of power mobility as the primary form of mobility on a daily basis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Peer Health Coaching Intervention
Intervention Arm - these participants receive individualized peer health coaching (intervention group only) and an adaptive physical activity guide of local resources (both groups)
|
Intervention arm: weekly sessions (~30 min each session) of physical activity counseling with an assigned peer health coach over the course of 12 weeks. The focus of the initial 2 calls is on rapport development and trust building with a focus around PA with discussion of physical activity goals and motives, where possible. The remainder of the call sessions follow a standardized format of a 30-minute call to 1) review the previous week, 2) integrate motivational strategies, and 3) develop action and support plans for the next week. The final call format includes a summary and evaluation of the intervention, discussion of short- and long-term goals, and relapse prevention strategies. Sessions guided by a call tracking form. These participants receive an adaptive physical activity local guide including information on local adaptive sports opportunities, which the control group also receives. |
|
No Intervention: Control
Control arm - these participants receive only an adaptive physical activity local guide including information on local adaptive sports opportunities however no individualized peer health coaching
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility measure: Recruitment
Time Frame: Months 1-12 for the overall study
|
Measuring feasibility of recruitment by measuring ability to reach goal of three to four participants/month are recruited over 12 months (for target n=40)
|
Months 1-12 for the overall study
|
|
Feasibility measure: Recruitment
Time Frame: Months 1-12 for the overall study
|
Measuring feasibility of recruitment by measuring ability to reach goal of >10% of eligible individuals approached for recruitment are recruited
|
Months 1-12 for the overall study
|
|
Feasibility: Stratification for age
Time Frame: Months 1-12 for the overall study
|
Measuring balance of recruitment by goal of intervention/control groups being balanced for age
|
Months 1-12 for the overall study
|
|
Feasibility: Stratification for sex
Time Frame: Months 1-12 for the overall study
|
Measuring balance of recruitment by goal of intervention/control groups being balanced for sex (male versus female)
|
Months 1-12 for the overall study
|
|
Feasibility: Stratification for diagnosis
Time Frame: Months 1-12 for the overall study
|
Measuring balance of recruitment by goal of intervention/control groups being balanced for diagnosis
|
Months 1-12 for the overall study
|
|
Feasibility: Attrition
Time Frame: Months 1-3 for participants; Months 1-15 of overall study
|
Measuring feasibility of participation by measuring ability to meet goal of having >80% of individuals complete all outcome measures
|
Months 1-3 for participants; Months 1-15 of overall study
|
|
Feasibility: Participant Engagement and Adherence to Intervention with Coach
Time Frame: Months 1-3 for intervention participants; Months 1-15 of overall study
|
Measuring feasibility of participant engagement and adherence to intervention by measuring ability of intervention group participants to complete the goal of >75% of calls with peer health coach
|
Months 1-3 for intervention participants; Months 1-15 of overall study
|
|
Feasibility: Participant Engagement and Adherence to Intervention: Post Call Questionnaires
Time Frame: Months 1-3 for intervention participants; Months 1-15 of overall study
|
Measuring feasibility of participant engagement and adherence to intervention by measuring ability of intervention group participants to complete the goal of >75% of post call questionnaires
|
Months 1-3 for intervention participants; Months 1-15 of overall study
|
|
Feasibility: Peer Health Coach Engagement and Implementation of Intervention: Checklist
Time Frame: Months 1-3 for intervention participants; Months 1-15 of overall study
|
Measuring feasibility of peer health coach engagement and implementation of intervention by measuring ability of Peer Health Coaches to complete the coaching intervention checklist with a goal of completion in >90% of sessions with intervention participant mentee
|
Months 1-3 for intervention participants; Months 1-15 of overall study
|
|
Feasibility: Peer Health Coach Engagement and Implementation of Intervention: Questionnaires
Time Frame: Months 1-3 for intervention participants; Months 1-15 of overall study
|
Measuring feasibility of peer health coach engagement and implementation of intervention by ability of peer health coaches to complete a goal of >90% of post call questionnaires
|
Months 1-3 for intervention participants; Months 1-15 of overall study
|
|
Feasibility: Peer Health Coach Engagement and Implementation of Intervention: Coaching Sessions
Time Frame: Months 1-3 for intervention participants; Months 1-15 of overall study
|
Measuring feasibility of peer health coach engagement and implementation of intervention by measuring the ability of Peer Health Coaches to complete full coaching session within 1 hour, including preparation, documenting call content, and post call questionnaires
|
Months 1-3 for intervention participants; Months 1-15 of overall study
|
|
Acceptability: Intervention Participants Qualitative Satisfaction with Peer Health Coach Intervention
Time Frame: Month 3 (after completion of intervention) for intervention participants
|
Measuring acceptability of peer health coach intervention through qualitative analysis of data from semi-structured interview.
After completion of intervention, each intervention participant has a semi-structured interview with the research team, with questions about satisfaction with peer health coach intervention.
|
Month 3 (after completion of intervention) for intervention participants
|
|
Acceptability: Intervention Participants Quantitative Satisfaction with Peer Health Coach Intervention
Time Frame: Month 3 (after completion of intervention) for intervention participants
|
Measuring acceptability of peer health coach intervention through a quantitative questionnaire with 3 questions that are using a scale of "No effort" to "Every Effort" regarding perceptions of the peer health coach's efforts in helping the intervention group participant meet their goals.
|
Month 3 (after completion of intervention) for intervention participants
|
|
Acceptability: Intervention Participants Qualitative Impact of Peer Health Coach Intervention
Time Frame: Month 6 (3 months post-intervention) for intervention participants
|
Measuring acceptability of peer health coach intervention through qualitative analysis of data from semi-structured interview.
Three months after completion of intervention, each intervention participant has a semi-structured interview with the research team, with questions about ongoing impact of peer health coaching intervention on removing physical activity barriers.
|
Month 6 (3 months post-intervention) for intervention participants
|
|
Acceptability: Intervention Participants Evaluation of Collaboration of the Peer Health Coach
Time Frame: Month 3 (after completion of intervention) for intervention participants
|
Measuring the quality of the peer health coach collaboration through survey question provided to the intervention group participants after completed of the intervention.
Percentage scale used from 0% to 100% rating of the collaboration, with higher numbers indicating greater collaboration.
|
Month 3 (after completion of intervention) for intervention participants
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Actigraph Electronic Physical Activity Tracker Compliance
Time Frame: Months 1-3 for participants; Months 1-15 of overall study
|
Measuring Actigraph Electronic Physical Activity Tracker compliance by measuring if compliance reaches a goal of 80% of participants assigned to wear Actigraph physical activity tracker (e.g., 50% of intervention group and 50% of control group) wearing the Actigraph at least 5 hours daily at least 4/7 days weekly averaged over a 4-week period throughout the 3-month period
|
Months 1-3 for participants; Months 1-15 of overall study
|
|
Arc Self-Determination Scale
Time Frame: At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
Self-determination will be evaluated via the Arc Self-Determination Scale (ASDS), which is reliable and valid in adolescents with disability.
There are 72 questions on the Arc Self-Determination Scale and the scoring is completed by taking raw values and comparing them against a normative value chart which then indicates the percentile of the scoring rather than using the raw values alone.
Higher percentiles indicate higher self determination.
|
At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
|
The PedsQL Measurement Model for the Pediatric Quality of Life Inventory
Time Frame: At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
This is a validated scale to measure quality of life (ages 5-18) in terms of school functioning and physical, emotional and social health.
This is well-researched in individuals with cerebral palsy and spina bifida.
The scale is from 0 to 100, with higher scores indicating higher health-related quality of life.
|
At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
|
Physical Activity Self-Efficacy Scale: Adolescent Protocol
Time Frame: At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
The Physical Activity Self-Efficacy Scale will test self-efficacy/confidence in physical activity engagement under challenging circumstances, and has good internal consistency and test-retest reliability.
The scale is from 8 to 40 with higher scores indicating higher self-efficacy.
|
At the following time points for participants: 6 weeks, 12 weeks, 6 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Cheri Blauwet, MD, Spaulding Rehabilitation Hospital
Publications and helpful links
General Publications
- Ryan RM, Deci EL. Self-determination theory and the facilitation of intrinsic motivation, social development, and well-being. Am Psychol. 2000 Jan;55(1):68-78. doi: 10.1037//0003-066x.55.1.68.
- Carbone PS, Smith PJ, Lewis C, LeBlanc C. Promoting the Participation of Children and Adolescents With Disabilities in Sports, Recreation, and Physical Activity. Pediatrics. 2021 Dec 1;148(6):e2021054664. doi: 10.1542/peds.2021-054664.
- Houlihan BV, Brody M, Everhart-Skeels S, Pernigotti D, Burnett S, Zazula J, Green C, Hasiotis S, Belliveau T, Seetharama S, Rosenblum D, Jette A. Randomized Trial of a Peer-Led, Telephone-Based Empowerment Intervention for Persons With Chronic Spinal Cord Injury Improves Health Self-Management. Arch Phys Med Rehabil. 2017 Jun;98(6):1067-1076.e1. doi: 10.1016/j.apmr.2017.02.005. Epub 2017 Mar 8.
- Houlihan BV, Everhart-Skeels S, Gutnick D, Pernigotti D, Zazula J, Brody M, Burnett S, Mercier H, Hasiotis S, Green C, Seetharama S, Belliveau T, Rosenblum D, Jette A. Empowering Adults With Chronic Spinal Cord Injury to Prevent Secondary Conditions. Arch Phys Med Rehabil. 2016 Oct;97(10):1687-1695.e5. doi: 10.1016/j.apmr.2016.04.005. Epub 2016 Apr 30.
- Kleis RR, Hoch MC, Hogg-Graham R, Hoch JM. The Effectiveness of the Transtheoretical Model to Improve Physical Activity in Healthy Adults: A Systematic Review. J Phys Act Health. 2021 Jan 1;18(1):94-108. doi: 10.1123/jpah.2020-0334. Epub 2020 Dec 1.
- Young MD, Plotnikoff RC, Collins CE, Callister R, Morgan PJ. Social cognitive theory and physical activity: a systematic review and meta-analysis. Obes Rev. 2014 Dec;15(12):983-95. doi: 10.1111/obr.12225. Epub 2014 Oct 7.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019P003354
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cerebral Palsy
-
Ankara City Hospital BilkentRecruitingCerebral Palsy (CP) | Cerebral Palsy, Spastic, Diplegic | Diplegic Cerebral Palsy With Spasticity | Transcranial Magnetic StimilationTurkey (Türkiye)
-
Lahore University of Biological and Applied SciencesRecruiting
-
Suleyman Demirel UniversityCompletedCerebral Palsy | Hemiplegic Cerebral Palsy | Spastic Diplegia Cerebral PalsyTurkey (Türkiye)
-
Holland Bloorview Kids Rehabilitation HospitalCanadian Institutes of Health Research (CIHR)RecruitingCerebral Palsy (CP) | Hemiplegic Cerebral PalsyCanada
-
Cairo UniversityCompletedCerebral Palsy (CP) | Unilateral Cerebral PalsyEgypt
-
University of California, San FranciscoNot yet recruitingCerebral Palsy | Cerebral Palsy (CP) | Infant | Cerebral Palsy InfantileUnited States
-
Lahore University of Biological and Applied SciencesNot yet recruitingSpastic Diplegia Cerebral PalsyPakistan
-
IRCCS Fondazione Stella MarisNot yet recruitingCerebral Palsy (CP) | EEG | Unilateral Cerebral Palsy | Action ObservationItaly
-
IRCCS Fondazione Stella MarisUniversity of Siena, ItalyRecruitingCerebral Palsy (CP) | Motor Imagery | CP (Cerebral Palsy) | Action ObservationItaly
-
Gazi UniversityCompletedCerebral Palsy | Cerebral Palsy, Spastic | Cerebral Palsy Spastic Diplegia | Cerebral Palsy Quadriplegic | Cerebral Palsy, MonoplegicTurkey
Clinical Trials on Virtual Peer Health Coaching
-
University of California, San FranciscoAmerican Academy of Family PhysiciansCompleted
-
Duke UniversityAdult Congenital Heart AssociationActive, not recruitingCongenital Heart Disease | Congenital Heart DefectUnited States
-
Slovak Academy of SciencesUniversity Hospital Bratislava Comenius University; Kempelen Institute of Inteligent...Recruiting
-
Emory UniversityNational Institute on Drug Abuse (NIDA)Not yet recruiting
-
Women's College HospitalUniversity Health Network, Toronto; Canadian Cancer Society (CCS); Public Health... and other collaboratorsActive, not recruitingCancer | Chronic DiseaseCanada
-
Brittany L SmallsNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)RecruitingDiabetes Mellitus, Type 2United States
-
VA Office of Research and DevelopmentActive, not recruitingHousing | Acute Care Service Utilization | Mental Health Status | Physical Health StatusUnited States
-
Tufts Medical CenterNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)Active, not recruitingFatigue | Systemic Lupus ErythematosusUnited States
-
Temple UniversityNational Institute on Disability, Independent Living, and Rehabilitation...CompletedSevere Mental DisorderUnited States
-
Medical College of WisconsinCompleted