Assessment of Body Composition, Fatigue, Mobility and Functional Status in Post-Stroke Individuals
1 other identifier
interventional
42
1 country
1
Brief Summary
The goal of this randomized controlled trial is to evaluate body composition, fatigue, mobility level, functional status in with stroke individuals. The main questions it aims to answer are: How is body composition affected in individuals with stroke? How is the level of fatigue affected in individuals with stroke? How is the mobility level affected in individuals with stroke? How is functional status affected in individuals with stroke? In this study, we included 21 patients with stroke and 21 healthy controls. The body composition of the participants was evaluated by Bioelectrical Impedance Analysis (BIA), fatigue level by Fatigue Severity Scale (FSS), mobility level by Rivermead Mobility Index (RMI), and functional status by Functional Independence Scale (FIM).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 17, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 5, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 5, 2022
CompletedFirst Submitted
Initial submission to the registry
October 14, 2023
CompletedFirst Posted
Study publicly available on registry
February 13, 2024
CompletedFebruary 13, 2024
February 1, 2024
6 months
October 14, 2023
February 2, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Bioelectrical Impedance Analysis
body weight
12 week
Bioelectrical Impedance Analysis
body fat percentage
12 week
Bioelectrical Impedance Analysis
muscle percentage
12 week
Bioelectrical Impedance Analysis
total water percentage
12 week
Bioelectrical Impedance Analysis
visceral fat amount
12 week
Bioelectrical Impedance Analysis
total bone mass
12 week
Secondary Outcomes (3)
Fatigue Severity Scale
12 week
Rivermead Mobility Index
12 week
Functional Independence Scale
12 week
Study Arms (2)
Experimental group
EXPERIMENTALIn all participants, body composition evaluation was carried out with the Beurer BF 1000 Super Precision device using the Bioelectrical Impedance Analysis principle, fatigue evaluation was carried out with the Fatigue Severity Scale, mobility evaluation was carried out with the Rivermead Mobility Index, and functional status evaluation was carried out with the Functional Independence Scale.
Control Group
ACTIVE COMPARATORIn all participants, body composition evaluation was carried out with the Beurer BF 1000 Super Precision device using the Bioelectrical Impedance Analysis principle, fatigue evaluation was carried out with the Fatigue Severity Scale, mobility evaluation was carried out with the Rivermead Mobility Index, and functional status evaluation was carried out with the Functional Independence Scale.
Interventions
Bioelectrical Impedance Analysis Beurer BF 1000 Super Precision device was used to measure the body composition of the participants. Operating on the principle of BIA, the device allows the body composition to be evaluated by giving an imperceptible electric current to the body. Fatigue Severity Scale (FSS) Fatigue Severity Scale (FSS) was used to measure participants' fatigue levels. Rivermead Mobility Index Rivermead Mobility Index (RMI) was used to assess the mobility levels of the participants. Functional Independence Measure Functional Independence Measure (FIM) was used to evaluate the functional status of the participants.
Eligibility Criteria
You may qualify if:
- Being between the ages of 18-65
- Volunteering to participate in the study
- Having a score of 25 or above on the Mini Mental Test
- Getting a score between 0-3 on the Modified Rankin Scale
You may not qualify if:
- Having cardiac insufficiency
- Being morbid obesity
- Having pacemaker
- Being pregnant
- Being between the ages of 30-65
- Volunteering to participate in the study
- Not having any neurological, orthopedic, rheumatologic and metabolic problems
- Having a score of 25 or above on the Mini Mental Test
- Participating in any fat burning diet program
- Exercising regularly
- Being pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pamukkale University
Denizli, 20160, Turkey (Türkiye)
Related Publications (33)
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MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Raziye Çelik, PT.
Pamukkale University
- STUDY DIRECTOR
Emre Baskan, Assoc Prof.
Pamukkale University
- STUDY DIRECTOR
Aziz Dengiz, PT Phd
Muş Alparslan University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator physiotherapist
Study Record Dates
First Submitted
October 14, 2023
First Posted
February 13, 2024
Study Start
December 17, 2021
Primary Completion
June 5, 2022
Study Completion
July 5, 2022
Last Updated
February 13, 2024
Record last verified: 2024-02