Clinical Trials Logo

Clinical Trial Summary

The objective of this study is to determine the effectiveness of remote manual wheelchair skills training program. First, peer coaches will be enrolled and trained. Then, trainees will be enrolled into one of three interventions: intervention with remote feedback (Group 1), wait list control group (Group 2), and structured self-study (Group 3).


Clinical Trial Description

For peer coaches: Coaches will complete the following measures pre and post training: - Demographic questionnaire - Self-Efficacy on Assessing, Training, and Spotting (SEATS) - Feedback survey Prior to coaching trainees, coaches will undergo three training programs as follows: - Virtual training through zoom on peer mentoring - Research ethics training - Wheelchair skills training It will be verified that peer coaches possess the needed skills by administering the SEATS following training. A score of 5 (completely confident) for each training item will be required to advance to the peer coaching sessions. For peer coaching, coaches will lead six 1:1 virtual zoom meetings with each trainee they are matched with. Sessions may include goal setting, review of progress, instruction, and "homework" of prescribed content for trainees to review. For each training session coaches will complete a session log. For trainees: Baseline questionnaires will include: - Demographic questionnaire - Wheelchair setup questionnaire - Wheelchair Skills Test Questionnaire (WST-Q) - Goal Attainment Scale (GAS) (Group 1,3 only) - Craig Handicap Assessment and Reporting Technique Short Form (CHART-SF) Mobility - Wheelchair Outcome Measure (WhOM) Satisfaction with Participation in Meaningful Activities - Life Space Assessment (LSA) - Online Learning Readiness Scale (OLRS) - Moorong Self-Efficacy Scale (MSES) - Referral Source - Wheelchair Skills Training Questionnaire - Wheelchair skills training outside of study Group Specific Activities Groups 1 and 2 will complete intervention A following baseline and 6-month assessments, respectively. Group 3 will complete intervention B. Participants in all groups will select what goals are important to them. They are not required to complete training in all skills, only to have at least 5 skills with relevant training goals. Intervention A Trainees will engage in 1:1 virtual zoom meetings facilitated by the study team scheduled weekly for 6 sessions with the opportunity for 2 makeup sessions. Sessions may include goal setting, review of progress, instruction, and "homework" of prescribed content for trainees to review. Participants may upload videos of themselves completing skills through Qualtrics to get feedback. Skills targeted by the intervention - 1. opening/closing doors 2. picking up an object from the ground 3. getting over a gap 4. getting over a threshold 5. up a low curb 6. down a low curb 7. up a high curb 8. down a high curb 9. performing a stationary wheelie 10. up a steep incline 11. down a steep incline 12. getting up stairs 13. getting down stairs 14. uneven transfers 15. floor-to-chair transfer 16. folding and unfolding wheelchair Intervention B Intervention B will be a series of educational videos that participants review and then are encouraged to practice the skills. Participants will have access to the materials for 8 weeks. Group 3 will have access to approximately 3 hours of wheelchair skills video training content. Actual viewing time will depend upon the individual's training goal. While they will receive a weekly reminder about practicing, there is no prescribed frequency for how often they should be practicing the skills in the videos. All participants will complete 2-month follow-up. This will include the following questionnaires: Baseline questionnaires will include: - Wheelchair setup questionnaire - Wheelchair skills training outside of study survey - Wheelchair Skills Test Questionnaire (WST-Q) - Goal Attainment Scale (GAS) - groups 1 and 3 only - Feedback Survey - groups 1 and 3 only - Wheelchair skills training outside of study All participants will complete 6-month follow-up. This will include the following questionnaires: - Wheelchair setup questionnaire - Wheelchair skills training outside of study survey - Wheelchair Skills Test Questionnaire (WST-Q) - Craig Handicap Assessment and Reporting Technique Short Form (CHART-SF) Mobility - Wheelchair Outcome Measure (WhOM) Satisfaction with Participation in Meaningful Activities - Life Space Assessment (LSA) - Wheelchair skills training outside of study Groups 2 will then cross-over to complete intervention A. All participants will complete 8-month follow-up. This will include the following questionnaires: - Wheelchair setup questionnaire - Wheelchair skills training outside of study survey - Wheelchair Skills Test Questionnaire (WST-Q) - Goal Attainment Scale (GAS) - group 2 only - Feedback Survey - group 2 only - Wheelchair skills training outside of study All participants will complete 12-month follow-up. This will include the following questionnaires: - Wheelchair setup questionnaire - Wheelchair Skills Test Questionnaire (WST-Q) - Craig Handicap Assessment and Reporting Technique Short Form (CHART-SF) Mobility - Wheelchair Outcome Measure (WhOM) Satisfaction with Participation in Meaningful Activities - Life Space Assessment (LSA) - Wheelchair skills training outside of study Follow-up windows will be within approximately 2 weeks before/after the follow-up date. Participants will be asked to select two preferred methods of contact for follow-up reminders that will be sent between timepoints. Spotters are required for trainee participation in the study. Prior to the start of the study, spotters will be required to watch a series of training videos about safe spotting. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06295146
Study type Interventional
Source University of Pittsburgh
Contact Lee Tempest, BS
Phone 412-232-9326
Email tempestml@upmc.edu
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date December 30, 2027

See also
  Status Clinical Trial Phase
Recruiting NCT04736849 - Epidural and Dorsal Root Stimulation in Humans With Spinal Cord Injury N/A
Terminated NCT00429013 - Pressure Ulcer Formation Prevention in Paraplegics Using Computer and Sensory Substitution Via the Tongue. Phase 2
Completed NCT00838838 - Efficacy of Nebido on Bone Mineral Density (BMD) in Hypogonadal Paraplegic Patients With Confirmed Osteoporosis N/A
Completed NCT05563402 - "Evaluation of Usability and Safety of the Self-balancing Walking System Atalante in Patients With Multiple Sclerosis" N/A
Recruiting NCT05432999 - Extracorporeal Shockwave Therapy for Spasticity in People With Spinal Cord Injury N/A
Enrolling by invitation NCT02602639 - Functional Electrical Stimulation With Rowing as Exercise After Spinal Cord Injury N/A
Completed NCT00385918 - Robotically Assisted Treadmill Training in Spinal Cord Injury (SCI) N/A
Recruiting NCT04397250 - High-intensity Interval Training for Cardiometabolic Health in Persons With Spinal Cord Injury N/A
Terminated NCT02412046 - Quantification of the Pressure Threshold Related to Tissue Injury in Bedriden Paraplegics N/A
Completed NCT06169969 - Effect Of Magnetic Therapy In Bladder Dysfunction And Quality Of Life In Paraplegic Patients N/A
Recruiting NCT01474148 - A Neuroprosthesis for Seated Posture and Balance N/A
Terminated NCT03114345 - Correlation Between Pressure Differences and Micro-vascularization Changes in Bedridden Paraplegic Patient N/A
Active, not recruiting NCT02600910 - Natural History of Shoulder Pathology in Manual Wheelchair Users
Completed NCT01739023 - Safety of Autologous Human Schwann Cells (ahSC) in Subjects With Subacute SCI Phase 1
Terminated NCT01498991 - Spinal Cord Injury Leg Rehabilitation Phase 1/Phase 2
Recruiting NCT06072001 - Long Term Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Central Neuropathy of Any Genesis Phase 3
Recruiting NCT06071949 - Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Central Neuropathy of Any Genesis Phase 3
Completed NCT04215081 - ExoAtlet II For SCI Patients N/A
Completed NCT04110561 - Evaluation of Safety and Performance of the Atalante System With Patients With Lower Limb Paralysis N/A
Completed NCT00270855 - Exercise to Reduce Obesity in Spinal Cord Injury N/A