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

NCT ID: NCT05159635

Last Updated: 2021-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-01

Study Completion Date

2019-10-01

Brief Summary

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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.

Detailed Description

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

Conditions

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Stroke Foot Drop (Acquired)

Keywords

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Wearable

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Active Living programme and wearable technical aids

Active Living programme and wearable technical aids

Group Type EXPERIMENTAL

Active Living programme and wearable technical aids

Intervention Type DEVICE

attend 6 weeks active living programme and apply wearable technical aids for 8 weeks.

Wearable technical aids

Wearable technical aids

Group Type ACTIVE_COMPARATOR

Wearable technical aids

Intervention Type DEVICE

apply wearable technical aids for 8 weeks.

Interventions

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Active Living programme and wearable technical aids

attend 6 weeks active living programme and apply wearable technical aids for 8 weeks.

Intervention Type DEVICE

Wearable technical aids

apply wearable technical aids for 8 weeks.

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kwong Wah Hospital

OTHER

Sponsor Role collaborator

Chinese University of Hong Kong

OTHER

Sponsor Role collaborator

Kowloon Hospital, Hong Kong

OTHER

Sponsor Role lead

Responsible Party

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Marko Chan

Senior Occupational Therapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Marko Chan, MSc

Role: PRINCIPAL_INVESTIGATOR

Community Rehabilitation Service Supoort Centre

Locations

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Community Rehabilitation Service Support Centre

Kowloon, , Hong Kong

Site Status

Countries

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Hong Kong

Other Identifiers

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KC/KE-17-0187/FR-3

Identifier Type: -

Identifier Source: org_study_id