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

NCT ID: NCT03828851

Last Updated: 2021-03-22

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

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-15

Study Completion Date

2018-09-20

Brief Summary

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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

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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.

Conditions

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Stroke

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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Experimental group

ADL training program.

Group Type EXPERIMENTAL

Domiciliary care - Activities of Daily Living

Intervention Type OTHER

Home-based ADL training.

Control group

Receive rehabilitation program in the hospital.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Domiciliary care - Activities of Daily Living

Home-based ADL training.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

20 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Der-Sheng Han, Doctor

Role: STUDY_CHAIR

National Taiwan University Hospital

Locations

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National Taiwan University Hospital

Taipei, Zhongzheng District, Taiwan

Site Status

Countries

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Taiwan

References

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Gibson E, Koh CL, Eames S, Bennett S, Scott AM, Hoffmann TC. Occupational therapy for cognitive impairment in stroke patients. Cochrane Database Syst Rev. 2022 Mar 29;3(3):CD006430. doi: 10.1002/14651858.CD006430.pub3.

Reference Type DERIVED
PMID: 35349186 (View on PubMed)

Other Identifiers

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201712067RIND

Identifier Type: -

Identifier Source: org_study_id

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