- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07401563
Community Mobility Plans: Improving Community Participation Through Travel Interventions for Adolescents and Young Adults With Intellectual and Developmental Disabilities
Enhancing Community Participation and Service Access for Transitional-Age Youth and Young Adults With Developmental Disabilities Through Community Mobility Plans
The goal of this study is to establish a proof-of-product by evaluating and refining the "Community Mobility Planning Process" curriculum activities with adolescents and young adults (AYA; ages 16-25 years) with Intellectual Disabilities (ID).
The main questions it aims to answer are:
- Is the Community Mobility Planning Process feasible to implement with adolescents and young adults with ID?
Participants will:
- Complete surveys and patient-reported outcome measures (PROMs) related to their experiences, attitudes, and feelings about community mobility.
- Complete a series of structured activities including worksheets, discussions, and specific skill building activities and share de-identified worksheets with the research team.
- Provide feedback about what they liked and didn't like about the the Community Mobility Planning Process.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
-
Gainesville, Florida, United States, 32611
- University of Florida
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Part of the program/classroom where professional plans to implement the Community Mobility Planning Process.
- 16-30 at start of implementation.
- Mild to moderate intellectual disability.
- Can participate in program activities in English.
Exclusion Criteria:
- Plan to end/stop participation in the current organization in <9 months from time of enrollment.
- A developmental disability without an intellectual disability
- Participants considered legally blind or deaf will be excluded to ensure a more homogeneous group for the initial development process
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Community Mobility Planning Process
|
The Community Mobility Planning Process (CMPP) consists of 5 steps to be implemented over an 8-week period.
The steps take a young adult with intellectual or developmental disabilities and their support staff through a series of activities to help them develop a plan to be more independent in their daily activities.
Step 1: Identify Person-Centered Community Mobility Priorities & Preferences (Weeks 1-4), Step 2: Evaluate Person & Environment Components Supporting Community Mobility (Weeks 5-8), Step 3: Set a Person-Centered Community Mobility Goal (Weeks 9-10), Step 4: Deliver Interventions to Support Community Mobility (Weeks 11-21), Step 5: Evaluate Progress (Weeks 22-24).
Each step has objectives and activities to support learning.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Community Mobility Experience
Time Frame: Pre-test, 1 month Post-test
|
This survey assesses how often and how easily individuals with intellectual and developmental disabilities (IDD) leave home to participate in daily activities.
It includes questions on transportation use, satisfaction, ease of access, and barriers or supports to community mobility.
Responses help inform transportation needs and evaluate mobility-related interventions.
The Community Mobility Experience Survey includes four scoring domains: frequency of community mobility (1-5), ease of mobility (1-4), sufficiency of mobility (0-2), and satisfaction with mobility (1-4).
Higher scores indicate greater frequency, ease, sufficiency, or satisfaction with community mobility.
In addition, specific transportation modes are evaluated across the same four domains-frequency, ease, sufficiency, and satisfaction-using the same scoring scales.
|
Pre-test, 1 month Post-test
|
|
Community Mobility Self-Efficacy
Time Frame: Pre-test, 1 month Post-test
|
This brief self-report measure assesses an individual's confidence in completing key steps related to community mobility and transportation planning.
The scale responses are informed by standards outline by Bandura's self-efficacy theory, and items are modified from the general self-efficacy scale.
Scores range from 20 to 60, with higher scores indicating a greater feeling of self-efficacy with community mobility.
|
Pre-test, 1 month Post-test
|
|
PROMIS Satisfaction with Participation and Discretionary Social Activities
Time Frame: Pre-test, 1 month Post-test
|
This brief PROM, available from PROMIS, evaluates satisfaction with level of involvement in leisure activities.
Scores range from 7 to 35, with higher scores indicating higher satisfaction with social roles and activities.
|
Pre-test, 1 month Post-test
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Beth Pfeiffer, PhD, OTR/L, BCP, FAOTA, Temple University
- Principal Investigator: Jessica Kramer, PhD, OTR/L, University of Florida
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 31078
- 901FDV0034-01-00 (Other Grant/Funding Number: Field Initiated Project, National Institute in Disability, Independent Living, and Rehabilitation Research (NIDILRR))
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 Intellectual and Developmental Disability
-
GalenusRx, Inc.CP UnlimitedNot yet recruitingDevelopmental Disability | Intellectual Disability, Mild | Intellectual Disability, Mild to ModerateUnited States
-
Temple UniversityUniversity of Florida; University of Minnesota; University of New HampshireNot yet recruitingDevelopmental Disability | Intellectual Disability, Mild to ModerateUnited States
-
University of Wisconsin, MadisonPatient-Centered Outcomes Research InstituteNot yet recruitingDevelopmental Disability | Intellectual DisabilitiesUnited States
-
Vestvagoy MunicipalityUniversity of Oslo; University of TromsoActive, not recruitingDisability, Developmental | Disabilities, IntellectualNorway
-
Albert Einstein College of MedicineNational Center for Advancing Translational Sciences (NCATS)RecruitingIntellectual Disability | Disability | Developmental DisabilityUnited States
-
Virginia Commonwealth UniversityNational Institute on Disability, Independent Living, and Rehabilitation...CompletedIntellectual Disability | Developmental DisabilityUnited States
-
University Hospital, MontpellierAssociation Xtraordinaire sub-group DDX3X; GenidaUnknownIntellectual Developmental Disorder | X-LINKEDFrance
-
University of Wisconsin, MadisonSyracuse University; University of Northern IowaCompleted
-
University of HaifaRecruitingIntellectual Disabilities Global Developmental DelayIsrael
-
University Hospital, MontpellierCompletedIntellectual Developmental Disorder | BCL11B Related DisorderFrance
Clinical Trials on Community Mobility Planning Process (CMPP)
-
Kean UniversityCompletedHealthyUnited States
-
Louisiana State University Health Sciences Center...University of California, Los Angeles; University of Southern California; National...CompletedDepression | Quality of Life | Anxiety | Social Stress | DisasterUnited States
-
McMaster UniversityCanadian Institutes of Health Research (CIHR); Public Health Agency of Canada... and other collaboratorsRecruitingHealthy Aging | Mobility Limitation | Health Related Quality of Life | Health InequityCanada
-
Oregon Health and Science UniversityUniversity of Colorado, Denver; University of Iowa; University of Wisconsin,...CompletedPatient Self-management Support
-
VA Office of Research and DevelopmentWithdrawn
-
Yale UniversityNational Institute of Mental Health (NIMH)Completed
-
Universidad Miguel Hernandez de ElcheRecruitingWell-being | Antibiotic Prescription | Health Literacy | Antimicrobial Drug Resistance | Health Equity | Social Capital | Cardio Vascular Disease | Community Based Participatory Research | Mental Health Literacy | Health-Related Quality-of-LifeSpain
-
St. Paul's Hospital Millennium Medical College,...Not yet recruitingPostpartum ContraceptionEthiopia
-
RANDMakerere UniversityNot yet recruitingFamily Planning
-
Planned Parenthood League of MassachusettsSociety for Family Planning Research FundCompletedFocus: Contraceptive Counseling | Focus: Postpartum ContraceptionPalestinian Territories, Occupied