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NCT05159635 Clinical Trial

Combining Active Living Programme (ALP) With Home-Use Wearable Technical Aids (WTA)

Stroke Clinical Trial

Official title:
The Effectiveness of Combining Active Living Programme (ALP) With Home-Use Wearable Technical Aids (WTA) to Promote Community Participation in Young Stroke With Foot Drop Problem- The Pilot Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05159635
Other study ID # KC/KE-17-0187/FR-3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2018
Est. completion date October 1, 2019

Study information
Verified date December 2021
Source Kowloon Hospital, Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to evaluate the effectiveness of adopting a home-use Wearable Technical Aids (WTA) with the structured Active Living Program (ALP) to promote community participation in young stroke patients.

Description:

Two groups of patients would receive Wearable Technical Aids Training or Wearable Technical Aids Training and structured Active Living Program (ALP) for 8 sessions.

Recruitment information / eligibility
Status Completed
Enrollment 12
Est. completion date October 1, 2019
Est. primary completion date June 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: -diagnosed with foot drop with tibialis anterior muscle strength between 1 to 3- out of 5 in manual muscle testing for more than six months due to cerebrovascular accident (CVA) Exclusion Criteria: - pre-existing orthopedic conditions affecting ambulation - subjects who are incompetent in giving written consent

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Active Living programme and wearable technical aids
attend 6 weeks active living programme and apply wearable technical aids for 8 weeks.
• Wearable technical aids
apply wearable technical aids for 8 weeks.

Locations
Country Name City State
Hong Kong Community Rehabilitation Service Support Centre Kowloon

Sponsors (3)
Lead Sponsor Collaborator
Kowloon Hospital, Hong Kong Chinese University of Hong Kong, Kwong Wah Hospital

Country where clinical trial is conducted

Hong Kong, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change score in Stroke Adapted 30 item version of the Sickness Impact Profile (SA-SIP 30) The quality of life scale for the people with stroke before intervention, 8 weeks (after intervention )
Secondary Change score in 10 meters walk Test 10 meters walk time before intervention,8 weeks (after intervention)
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