Studying Rehabilitation Treatments Using Video to Improve Recovery for Adults With Physical Disabilities
Using the Rehabilitation Treatment Specification System (RTSS) to Maximize Rehabilitation Research Impact: A Video-Based Observational Study
2 other identifiers
observational
90
1 country
1
Brief Summary
This study aims to better understand how occupational therapists provide rehabilitation for adults recovering from stroke or spinal cord injury (SCI), with a focus on improving arm and hand function. Using video recordings of real outpatient therapy sessions, researchers will identify the key elements of treatment, such as the types of activities, the therapist's techniques, and how patients respond. The study will use the Rehabilitation Treatment Specification System (RTSS), a framework designed to clearly describe rehabilitation methods. By analyzing these sessions, the research team will develop a practical toolkit to help therapists and researchers deliver and study more effective rehabilitation treatments in the future.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 11, 2025
CompletedFirst Submitted
Initial submission to the registry
June 17, 2025
CompletedFirst Posted
Study publicly available on registry
July 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
December 18, 2025
December 1, 2025
1.5 years
June 17, 2025
December 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time Spent on Different Types of Treatment Activities
We will quantify time spent in different treatment types during standard care occupational therapy, as specified in the Rehabilitation Treatment Specification System.
Through study completion, Up to 24 months
Secondary Outcomes (2)
Feasibility of Video Recording Intervention
Following participant data collection/video recording through study completion, up to 24 months
Acceptability of Video Recording Intervention
Following participant data collection/video recording through study completion, up to 24 months
Study Arms (3)
Occupational Therapy Practitioners
Occupational therapists and occupational therapy assistants employed by OSU Wexner Medical Center
Spinal Cord Injury
Spinal cord injury patients receiving outpatient OT at OSUMC
Stroke
Stroke patients receiving outpatient OT at OSUMC
Interventions
N/A as there is no intervention for this study
Eligibility Criteria
A purposive sample of OT practitioners working in an outpatient rehabilitation at OSUWMC will be recruited for this study. A purposive sample of stroke patients receiving OT at an OSU outpatient rehabilitation clinic will be recruited for this study. A purposive sample of SCI patients receiving OT at an OSU outpatient rehabilitation clinic will be recruited for this study.
You may qualify if:
- Must be a licensed OT practitioner (occupational therapist or occupational therapy assistant),
- The OT practitioner must treat at least one adult stroke or spinal cord injury patient with UE sensorimotor impairment per month
- The OT practitioner must be willing to be video recorded while treating their enrolled stroke or SCI patients.
- Must have a medical diagnosis of ischemic or hemorrhagic stroke
- Must be ≥ 18 years old
- Must have at least one OT goal related to UE hemiparesis
- Must have at least one remaining OT treatment session after enrollment
- The patient's OT must be enrolled in the study.
- Must have a medical diagnosis of cervical spinal cord injury
- Must be ≥ 18 years old
- Must have at least one OT goal related to UE sensorimotor impairment
- Must have at least one remaining OT treatment session after enrollment
- The patient's OT must be enrolled in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ohio State Universitylead
- American Occupational Therapy Foundationcollaborator
Study Sites (1)
Ohio State Wexner Medical Center
Columbus, Ohio, 43210, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 17, 2025
First Posted
July 29, 2025
Study Start
February 11, 2025
Primary Completion (Estimated)
July 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
December 18, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share