Comparison of the Effectiveness of Intradialytic Core Stabilization and Aerobic Exercise in Hemodialysis Patients
NCT ID: NCT05534542
Last Updated: 2024-06-04
Study Results
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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COMPLETED
NA
40 participants
INTERVENTIONAL
2022-08-01
2022-10-07
Brief Summary
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Materials and Methods: Patients who received hemodialysis treatment for 4 hours, 3 days a week were planned to be included in this randomized controlled study. Patients participating in the study will be randomly divided into 2 groups. Grup 1 was planned to be given core stabilization exercises during hemodialysis three times a week for eight weeks; Group 2 was planned to be given aerobic exercise during hemodialysis three times a week for eight weeks. It aimed to evaluate the patients in the weeks before the start of the treatment and the week after the end of the treatment. Personal information form for evaluation, dialysis adequacy, quality of life questionnaire-kidney disease quality of life-36, piper fatigue scale, hospital anxiety and depression scale (hads), Pittsburgh sleep scale, five times sit and stand test, 10 m walking test , tinetti balance and walking test, and 2-minute step test were planned to be used.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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core stabılızatıon
use of ıntradıalıtıc core stabılızatıon ın hemodıalysıs patıents
exercıse
ıntradıalıtıc core stabılızatıon
aerobıc exercıse
use of ıntradıalıtıc aerobıc exercıse ın hemodıalysıs patıents
exercıse
ıntradıalıtıc core stabılızatıon
Interventions
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exercıse
ıntradıalıtıc core stabılızatıon
Eligibility Criteria
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Inclusion Criteria
* Being 18 years or older
* A score of 3 and/or below in the Sarcopenia Screening Test (SARC-F)
Exclusion Criteria
* Having angina pectoris, arrhythmia, or uncontrolled hypertension
* Having communication and/or cognitive issues that prevent them from meeting the requirements of the tests
* Becoming pregnant or going through infertility treatment
* Having a psychiatric diagnosis
18 Years
80 Years
ALL
No
Sponsors
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Muş Alparslan University
OTHER
Responsible Party
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Principal Investigators
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Cengiz TAŞKAYA
Role: PRINCIPAL_INVESTIGATOR
scholar
Buket Büyükturan
Role: STUDY_DIRECTOR
scholar
Locations
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Mus State Hospital
Muş, Muş, Turkey (Türkiye)
Countries
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Other Identifiers
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cngztaskaya
Identifier Type: -
Identifier Source: org_study_id
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