- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06156813
Turkish Lower-Extremity Motor Activity Log (LE-MAL)
Validity and Reliability of Turkish Version of the Lower Extremity Motor Activity Log
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The Motor Activity Log was developed to measure paretic upper extremity use in daily activities in the real-life context (real world) of people with different health conditions, including stroke. Real-world use outside the individual's clinical/laboratory environment, including daily activities (e.g., walking indoors and outdoors above ground, climbing stairs, getting in and out of a car, jumping over an object, picking up an object, sitting and standing) It's about what they do.
The Motor Activity Log is a reliable patient self-report measure and correlates significantly with another real-world measure, the accelerometer.
Adaptation of the Motor Activity Log to the lower extremity involved the development of three subscales to measure changes in types of activity that are bilateral in nature and use of the paretic lower extremity: level of assistance, functional ability, and confidence. The Lower Extremity Motor Activity Log is a semi-structured questionnaire in which the participant is asked to rate himself on each scale across 14 activities. The score for each scale is the average of the rate provided for each activity. Additionally, a composite score can be calculated that combines all scales through assistance, functional ability, and confidence scores.
A preliminary study with individuals with stroke using the English version of the Lower Extremity Motor Activity Log-14 showed that the total score was 0.93, 0.90, 0.94, and 0.88 test-retest for the composite score, assistance, functional ability, and confidence scales, respectively. The test showed that it has reliability.
The aim of this study is to investigate the reliability and validity of the Turkish version of the Lower Extremity Motor Activity Log-14.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Zekiye İpek Katırcı Kırmacı, PhD
- Phone Number: +90 544 261 82 85
- Email: ipekkatirci@hotmail.com
Study Locations
-
-
-
Gaziantep, Turkey
- Recruiting
- Gaziantep Islam Science and Technology University
-
Contact:
- Zekiye İpek Katırcı kırmacı
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals between the ages of 18-80 living in Gaziantep who applied to the neurology outpatient clinic of Hospital and were diagnosed with stroke.
Exclusion Criteria:
- Patients with a history of trauma within the last year, alcohol and substance addiction, and pregnancy
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Tr- LE-MAL
Time Frame: baseline and two weeks later
|
t is a semi-structured interview that includes questions to determine the participant's level of assistance, movement quality and confidence while performing a 14-day activity.
|
baseline and two weeks later
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroke Impact Scale
Time Frame: Baseline
|
This scale, which aims to evaluate the perception of the quality of life after stroke by the patients themselves or their caregivers, consists of 8 subsections and 59 questions.
|
Baseline
|
6 min walk test
Time Frame: Baseline
|
Functional capacity in terms of mobility is evaluated by measuring the person's maximum walking distance within a six-minute period.
|
Baseline
|
Collaborators and Investigators
Investigators
- Principal Investigator: Zekiye İpek Katırcı Kırmacı, Gaziantep Islam Science and Technology University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ipek.kirmaci
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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