Viewing Study NCT06294834



Ignite Creation Date: 2024-05-06 @ 8:13 PM
Last Modification Date: 2024-10-26 @ 3:22 PM
Study NCT ID: NCT06294834
Status: RECRUITING
Last Update Posted: 2024-03-06
First Post: 2024-02-27

Brief Title: Improving Clinician Capacity to Provide Interventions for Manual Wheelchair Users
Sponsor: University of Pittsburgh
Organization: University of Pittsburgh

Study Overview

Official Title: Improving Clinician Capacity to Provide Interventions for Manual Wheelchair Users
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SKILL
Brief Summary: The objective of this study is to determine the effectiveness of remote manual wheelchair skills training program for clinicians The study will use three-group approach intervention with remote feedback Group 1 control group Group 2 and structured self-study Group 3 This demonstrates how the intervention compares not only to a control but also to the next best alternative - therapists sourcing web-based training materials and learning independently
Detailed Description: A randomized single-blinded two-period cross-over study design for Groups 1 and 2 will be used Participants will complete baseline assessments and then be randomized to either Group 1 or Group 2 After enrollment for Groups 1 and 2 is completed Group 3 participants will be enrolled

Group 1 will receive the active intervention intervention A which will include a two-part training in wheelchair skills For Part 1 they will review approximately 4 hours of educational videos on how to complete and teach wheelchair skills For Part 2 they will complete a practice-feedback loop with a remote trainer providing asynchronous feedback Group 3 will mirror Group 1 but complete only Part 1 of the training Group 2 will receive the control intervention intervention B participants will review approximately 4 hours of educational videos Participants will have 8 weeks to complete either training program Both groups will then complete follow-up at 2 and 6 months Following this participants will cross over to receive the other intervention Group 1 and 3 will receive intervention B Group 2 will receive intervention A and complete follow-up at 8 and 12 months

Additionally rehabilitation professionals who are not therapists will be able to access the training through a structured self-study Group 4 This group will receive access to both trainings with follow-up at 2 and 6 months

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
90SIMS0010 OTHER_GRANT NIDILRR None