Effectiveness of Web-Based Training (SERT)

Not Applicable

Active, not recruiting

• Conditions: Remote Transfer Training Program
• Interventions: Behavioral: Independent Transfer Training

• Registration Number: NCT03164278
• Lead Sponsor: University of Pittsburgh

Brief Summary

The objective of this research study is to assess the effectiveness of an independent transfer training program (ITTP), and to determine methods which may increase overall success of an online training program.

Detailed Description

Up to 200 individuals will be recruited for this research study. Investigators will recruit individuals who use a wheelchair for the majority of their mobility (over 40 hours per week), have the ability to transfer independently (may use equipment like sliding boards), use a seated pivot to transfer, and speak English as a primary a language. This study will be accessed entirely online and participation is expected to last approximately one year. Subjects will be randomized into three groups; one group that will receive transfer training immediately with no follow up, one group that will receive the transfer training immediately with 1 month and 6 month follow up, and one group that will receive the transfer training after 6 months. The transfer training program itself will take approximately 1 hour to complete.

After obtaining informed consent, participants in the first two groups will complete baseline questionnaires. They will then receive the transfer training program.

Participants in the third group (a wait-list control group) will complete the baseline questionnaires and be contacted one month later to complete a transfer assessment instrument questionnaire. They will then wait 5 months. After this period, participants will complete the baseline questionnaires a second time, and then receive the transfer training.

After completing the transfer training, all groups will be contacted immediately post training to complete additional questionnaires to assess the effectiveness of the remote transfer training program. Participants in the 2nd and 3rd group will be contacted 1 month and 6 months post-training to complete additional questionnaires.

Study Timeline

• Study First Submitted: 2017-05-18
• Study First Submitted QC: 2017-05-19
• Study First Posted: 2017-05-23
• Study Start: 2017-12-04
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-27
• Last Update Posted: 2025-03-03
• Primary Completion: 2025-12-01
• Study Completion: 2026-12-01

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

1. Utilize a wheelchair for the majority of mobility (over 40 hours per week).
2. Ability to transfer independently (may use equipment like sliding boards).
3. Use of seated pivot transfer
4. Speak English as a primary a language

Exclusion Criteria

1. Pain prohibiting transfers
2. Active use of the lower limb muscles during transfers
3. Current or recent history (last 3 months) of pressure sores

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Randomized Training	Independent Transfer Training	Individuals may decide to participate in the research study and agree to be randomized. These individuals will be immediately randomized into an immediate or a wait list control group. The immediate will receive the independent transfer training program after completing the baseline questionnaires. The wait list control group will wait approximately 6 months before receiving the independent transfer training program.
Immediate Training (no follow up)	Independent Transfer Training	Individuals may decide to participate in the research study training program, but not in any follow up questionnaires. This group will have immediate access to the independent transfer training materials. They will complete data collection measures embedded in the transfer training program, including demographics, Online Learning Readiness Scale (OLRS), Moorong Self Efficacy Scale (MSES), Patient Reported Outcome Measurement Information System (PROMIS), Transfer Assessment Instrument Questionnaire (TAI-Q), and the Wheelchair User Shoulder Pain Index (WUSPI).
Immediate Training (with follow up)	Independent Transfer Training	Individuals may decide to participate in the research study, but do not want to be randomized. After consent is obtained, these individuals will be directed immediately to the baseline questionnaires (see above) before and after the independent transfer training. Participants may also be asked to complete a user satisfaction survey.

Primary Outcome Measures

Name	Time	Method
Change in Transfer Assessment Instrument Questionnaires (TAI-Q)	This measure is collected at baseline, pre- training, during the training, as well as at the 1 month and 6 month follow ups.	We will assess the mathematical difference in assessments from baseline to follow-up.

Secondary Outcome Measures

Name	Time	Method
Change in Patient Reported Outcomes Measurement Information System: Physical Function with Mobility Aid	This measure is collected pre-training and at the 6 month follow up.	We will assess the mathematical difference in assessments from baseline to follow-up.
Change in Wheelchair Users Shoulder Pain Index (WUSPI)	This measure is collected pre- training, as well as at 6 month follow up.	We will assess the mathematical difference in assessments from baseline to follow-up.
Change in Patient Reported Outcomes Measurement Information System: Satisfaction with Social Roles & Activities	This measure is collected pre-training and at the 6 month follow up.	We will assess the mathematical difference in assessments from baseline to follow-up.
Change in Patient Reported Outcomes Measurement Information System: Ability to Participate in Social Roles and Activities	This measure is collected pre-training and at the 6 month follow up.	We will assess the mathematical difference in assessments from baseline to follow-up.

Trial Locations

Locations (1)

University of Pittsburgh; 🇺🇸 Pittsburgh, Pennsylvania, United States