- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06323850
Improving Access to Community-Based Occupations Via a Rideshare Training Program
Improving Access to Community-Based Occupations Via a Rideshare Training Progra
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Rideshare services are widely adopted across the globe and provide a safer, more flexible, and less taxing transportation option for many individuals. Rideshare can help people to get to more places they want to go and allows for spontaneity since a ride can be arranged in the moment, at any time of day. Rideshare picks passengers up and drops them off at their specific destination, eliminating the need to walk to bus stops, wait at stations, or transfer to more than one bus or train. Not only does this save time, it may increase safety especially at night or during inclement weather. Rideshare may also be more reliable for getting to work on time. Finally, while communicating with the driver may be a challenge, there is only one person with which to interact versus potentially many people waiting at stations or on the bus or train.
While the use of Rideshare has the potential to improve community access and expand occupational engagement for autistic adults, few training resources exist to introduce clients to this mode of transportation, assess readiness, or build confidence. Our Rideshare training program has proven feasible to conduct with autistic adults living in an urban-based semi-structured independent housing residence. This study will test the effectiveness and implementation of the SRP program in a wider range of autistic adults living in the central Virginia region
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Virginia
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Richmond, Virginia, United States, 23298
- Virginia Commonwealth University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- study participants have to be 18+ years of age
- living within 100 miles of Richmond, Virginia
- Participants have to have diagnosis of ASD given by a licensed medical professional.
- Participants need to have a stable internet connection
- ability to communicate independently (verbally or via alternative communication device) in English
- have the motoric skills needed to independently use a smartphone (fine motor) and get in and out of a car (gross motor).
- Participants must own a smartphone and be familiar with texting and/or email.
Exclusion Criteria:
- participants who have a severe or profound intellectual disability (IQ below 35) given that the training was designed for those with moderate IQ and above with the potential to travel alone to familiar places
- exclude any individual who already uses Rideshare independently.
- exclude pregnant women.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
The experimental group will receive the intervention then a 2-month follow-up
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After participants have been enrolled, they will be assigned to one of the trainer-pairs and will work with them to schedule the first two sessions.
Most clients will be able to schedule one virtual session per week and one ride along session per week for the first five weeks, with the remaining three weeks allotted to practice ride-along sessions and module repetition (as needed).
The additional time also provides a buffer if subjects are unavailable for a week during the intervention phase.
Virtual sessions will take place over Zoom each session lasting 20-30 minutes.
Each of the five virtual sessions will be aligned with the five online modules.
For each module, exercises are built in to test comprehension.
If the participant does not complete an exercise accurately, the lead trainer will explain why the response was incorrect and prompt them to repeat the video modeling exercise.
The support training partner will take notes to support the formative assessment process and complete fidelity checks.
The first ride-along session will be the baseline session for assessing level of independence (number of cues needed) and safety.
The participant will have up to 8 ride-along sessions to reach full independence (no cues needed) and full marks on the safety assessment.
The lead trainer will provide the cues as needed to complete each step of the Rideshare process.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluate if the trainers conducting the SRP intervention find the intervention to be appropriate
Time Frame: Baseline and after phase 1 (5 weeks)
|
Trainers conducting the SRP intervention will rate 75% of the items on the Intervention Appropriateness Measure (IAM) as Agree or Completely Agree.
The AIM is a 5-item scale that measures the perception among implementation stakeholders that a given treatment, service, practice, or innovation is agreeable, palatable, or satisfactory.
Acceptability refers to determining how well an intervention will be received by the target population and the extent to which the new intervention or its components might meet the needs of the target population and organizational setting.
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Baseline and after phase 1 (5 weeks)
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Evaluate autistic adults participating in the SRP intervention find the intervention acceptable?
Time Frame: Baseline and after phase 1 (5 weeks)
|
Autistic adults participating in the SRP will rate 75% of the items on the Acceptability Intervention Measure (AIM) as Agree or Completely Agree.
The AIM is a 5-item scale that measures the perception among implementation stakeholders that a given treatment, service, practice, or innovation is agreeable, palatable, or satisfactory.
Acceptability refers to determining how well an intervention will be received by the target population and the extent to which the new intervention or its components might meet the needs of the target population and organizational setting.
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Baseline and after phase 1 (5 weeks)
|
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Autistic adults who have participated in the SRP program display greater independence in using Rideshare
Time Frame: Baseline and after phase 1 (5 weeks)
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Autistic adult who have participated in the SRP program will display greater independence in using Rideshare
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Baseline and after phase 1 (5 weeks)
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Autistic adults who have participated in the SRP program display greater safety in using Rideshare
Time Frame: Baseline and after phase 1 (5 weeks)
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Autistic adult who have participated in the SRP program will display greater safety when using Rideshare
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Baseline and after phase 1 (5 weeks)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
How do SRP participants use of Rideshare for community, social, and/or employment activities after the intervention
Time Frame: Baseline and after phase 1 (5 weeks) and 3 months post intervention
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This is an exploratory research question and the investigators will use descriptive statistics and visual analyses to look at trends in how Rideshare is used after participation in the SRP program.
The investigators will also gather qualitative data through post-intervention interviews with participants to help determine the impact of the program and what improvements are needed.
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Baseline and after phase 1 (5 weeks) and 3 months post intervention
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Stacey Reynolds, Virginia Commonwealth University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- HM20028878
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.
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