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Clinical Trials/NCT03828851
NCT03828851CompletedNot Applicable

Development of Domiciliary Program on Improving Activities of Daily Living Program for Patients With Stroke

National Taiwan University Hospital1 site in 1 country26 target enrollmentStarted: February 15, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
26
Locations
1
Primary Endpoint
Changes of the Canadian Occupational Performance Measure

Study Overview

Brief Summary

The purpose of this study was to investigate the effects of the Domiciliary care- Activities of Daily Living program on activities of daily living (ADL), motor, cognition, perception, sensory, quality of life, and depression for patients with stroke.

Detailed Description

Administering ADL and recovery of ADL functions are the primary efficacy indicators in long-term care and the main treatment goals in rehabilitation for patients with stroke. Residential rehabilitation is a direct way to observe patients' living environment and provides feasible ADL treatment plans for patients with stroke living at home or in the community. The purpose of this study was to investigate the effects of the Domiciliary care- Activities of Daily Living program on activities of daily living, motor, cognition, perception, sensory, quality of life, and depression. The eligible participants were recruited and assigned into two groups: ADL home program and control group who received traditional rehabilitation in hospital. The primary outcome measures were the Canadian Occupational Performance Measure, the Barthel Index-based Supplementary Scales, the Frenchay Activities Index, and ADL domain of the Stroke Impact Scale. The secondary outcome measures were the Fugl-Meyer Assessment, the Mini Mental State Examination, the Test of Visual Perceptual Skills-Third Edition, and the Center of Epidemiological Study-Depression.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosis of stroke
  • •Aged > 20 years
  • •Score 2-4 of the modified Rankin Scale
  • •Capability of following instructions
  • •Willing to participants to the study

Exclusion Criteria

  • •Diagnoses of dementia and Parkinson's disease
  • •Physical limitations because of orthopedics diseases
  • •Peripheral nerve injury

Arms & Interventions

Control group

No Intervention

Receive rehabilitation program in the hospital.

Experimental group

Experimental

ADL training program.

Intervention: Domiciliary care - Activities of Daily Living (Other)

Outcomes

Primary Outcomes

Changes of the Canadian Occupational Performance Measure

Time Frame: 6 months

The Canadian Occupational Performance Measure assesses occupational performance. The total score ranges from 1-10. A higher score indicates better occupational performance. Changes of occupational performance will be assessed at the 6 weeks, 12 weeks, and 6 months.

Changes of the Barthel Index-based Supplementary Scales

Time Frame: 6 months

The Barthel Index-based Supplementary Scales assesses basic activities of daily living. The total score range from 0-58. A higher score indicates better basic activities of daily living. Changes of basic activities of daily living will be assessed at the 6 weeks, 12 weeks, and 6 months.

Changes of the Frenchay Activities Index

Time Frame: 6 months

The Frenchay Activities Index assesses instrumental activities of daily living. The total score range from 0-45. A higher score indicates better instrumental activities of daily living. Changes of instrumental activities of daily living will be assessed at the 6 weeks, 12 weeks, and 6 months.

Changes of the ADL domain of the Stroke Impact Scale

Time Frame: 6 months

The ADL domain of the Stroke Impact Scale assess difficulty in performing activities of daily living. The domain score range from 10-50. A higher score indicates less difficulty in performing activities of daily living. Changes of difficulty in performing activities of daily living will be assessed at the 6 weeks, 12 weeks, and 6 months.

Secondary Outcomes

  • Changes of the Fugl-Meyer Assessment(6 months)
  • Changes of the Mini Mental State Examination(6 months)
  • Changes of the Center of Epidemiological Study-Depression(6 months)
  • Changes of the Test of Visual Perceptual Skills-Third Edition(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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