Skip to main content
OpenTrials
Completed

NCT Number: NCT04399759

Instrumental Activities of Daily Living Approach in Home Environment for Patients With Stroke

The purpose of this study was to conduct a randomized clinical trial. Implement instrumental daily activities of daily living (A-IADL) in home rehabilitation. To explore the effect of A-IADL on stroke patients' movement, cognition, social participation, daily life function and quality of life.

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cardinal Tien Hospital

New Taipei City, Xindian Dist, 231403, Taiwan

About this study

Subjects were randomized to intervention group and control group. The experiment was designed as randomized cross-over control trial. The primary outcome included 11 measures, Fugl-Meyer Assessment, Balance computerized adaptive testing, Mini Mental State Examination, Participation Measure-3 Domains ,4 Dimensions, Canadian Occupational Performance Measure, Barthel Index-based Supplementary Scales, Frenchay Activities Index, Lawnton Instrumental Activities of Daily Living, stroke impact scale, Stroke Self-Efficacy Questionnaire, and Kingston Caregiver Stress Scale.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age > 20 years
  • Diagnosis of stroke
  • The modified Rankin Scale : 2~4
  • Keep sitting for half an hour by himself/herself
  • Follow instructions
  • Willing to sign the subject's consent

Exclusion criteria

  • Diagnosis of dementia
  • History of orthopedic diseases or peripheral nerve injury

Treatment and study plan

Approach-Instrumental Activities of Daily Living

Behavioral

Individualized instrumental activities of daily living training

Home health education

Behavioral

Individualized home health education

Primary outcomes

  1. Fugl-Meyer Assessment

    Time frame: Baseline to 6 weeks

    The Fugl-Meyer Assessment scale is an index to assess the sensorimotor impairment in individuals who have had stroke. The score ranges is 0 to 226. A higher score indicates better body function.

  2. Balance computerized adaptive testing

    Time frame: Baseline to 6 weeks

    The Balance computerized adaptive testing is a test about stroke patients, includes movement, balance, activities of daily living.

  3. Mini Mental State Examination

    Time frame: Baseline to 6 weeks

    The Mini Mental State Examination general cognitive function. The score ranges is 0 to 30. A higher score indicates better general cognitive function.

  4. Participation Measure-3 Domains ,4 Dimensions

    Time frame: Baseline to 6 weeks

    The Participation Measure-3 Domains, 4 Dimensions assesses social participation. A higher score indicates better social participation.

  5. Canadian Occupational Performance Measure

    Time frame: Baseline to 6 weeks

    The COPM protocol is divided into three areas: self-care, productivity, and leisure. Patients define important activities and classify them with a score of one to 10. A higher score indicates better occupational performance.

  6. Barthel Index (BI) -based Supplementary Scales

    Time frame: Baseline to 6 weeks

    The Barthel Index-based Supplementary Scales assesses basic activities of daily living using three scales:actual performance, ability, and self-perceived difficulty. The score ranges the three scales (i.e., actual performance, ability, and self-perceived difficulty)is 0-20, 0-18, and 0-20, respectively. A higher score indicates better basic activities of daily living.

  7. Frenchay Activities Index

    Time frame: Baseline to 6 weeks

    The Frenchay Activities Index is a measure of instrumental activities of daily living for use with patients recovering from stroke. The score ranges is 0 to 45. A higher score indicates better instrumental activities of daily living.

  8. Lawnton Instrumental Activities of Daily Living

    Time frame: Baseline to 6 weeks

    The Lawnton Instrumental Activities of Daily Living assesses instrumental activities of daily living.The score ranges is 0 to 8. A higher score indicates better instrumental activities of daily living.

  9. Stroke Impact Scale

    Time frame: Baseline to 6 weeks

    The Stroke Impact Scale assesses other dimensions of health-related quality of life: emotion, communication, memory and thinking, and social role function.The score ranges is 59 to 295. A lower score indicates the quality of life less affected by stroke.

  10. Stroke Self-Efficacy Questionnaire

    Time frame: Baseline to 6 weeks

    The Stroke Self-Efficacy Questionnaire is a self-report scale measuring self-efficacy judgments in specific domains of functioning post stroke. The score ranges is 0 to 130. A higher score indicates better self-efficacy.

  11. Kingston Caregiver Stress Scale

    Time frame: Baseline to 6 weeks

    The Kingston Caregiver Stress Scale is a self-report scale measuring caregiver stress. The score ranges is 10 to 50. A higher score indicates greater stress.

Sponsors and collaborators

Lead sponsor

National Taipei University of Nursing and Health Sciences

Other

Registry information

Official study title

Investigation of the Effect on Instrumental Activities of Daily Living Approach in Home Environment for Patients With Stroke

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
May 22, 2020
Registry last updated
Jul 28, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.