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Self-Management for Amputee Rehabilitation Using Technology

NCT04120038 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2021-10-15

No results posted yet for this study

Summary

The purpose of this study is to determine the effect of 6 weeks of the SMART Program on the walking capacity and confidence of individuals with unilateral lower limb amputation (LLA). Our primary hypothesis is that SMART can improve walking capacity in individuals with LLA. Our secondary hypothesis is that SMART can improve ambulation confidence, body function, depression, body image, pain, balance confidence, activities of daily living, satisfaction with life and habit formation for skin monitoring and prosthetic cleaning in individuals with LLA. A post-intervention one on one interview will be conducted to understand SMART acceptability. The entirety of the study, including intervention administration, assessment, and interviews will be conducted online.

Conditions

  • Unilateral Trans Tibial/Femoral Lower Limb Amputation

Interventions

DEVICE

Self-Management for Amputee Rehabilitation using Technology [SMART]

Participants will complete a 6-week tablet-based education program for individuals with LLA that will provide them with self-management education.

Sponsors & Collaborators

  • Vancouver Coastal Health Research Institute

    collaborator OTHER

  • GF Strong Rehabilitation Centre

    collaborator OTHER

  • University of British Columbia

    lead OTHER

Principal Investigators

  • William C Miller, PhD · University of British Columbia

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-26
Primary Completion
2021-08-31
Completion
2021-08-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04120038 on ClinicalTrials.gov