The Effect of Self Acupressure in Patients With Multiple Sclerosis
NCT ID: NCT06600971
Last Updated: 2024-10-16
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
2024-03-18
2024-09-03
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
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acupressure
The patients in the experimental group received acupressure application for a total of 8 sessions, 2 sessions per week. The first application was performed in a room in the polyclinic by a researcher with an acupressure application certificate. Immediately after the preparation phase, the researcher applied acupressure with the thumb in a certain order (Ht7-Ht7 and St36-St36) on each point to be pressed, in accordance with the acupressure application protocol, for a duration of 2 minutes. Verbal communication was maintained during the procedure to ensure the patient's relaxation. After the first application, the application was taught to the patient. In addition, the researcher established a WhatsApp group for regular follow-up of the patients in the experimental group, and the video recording of the acupressure was sent to the patients and they were asked to watch it.
acupressure application
The patients in the experimental group received acupressure application for a total of 8 sessions, 2 sessions per week.
Control
During the study, it was explained to the control group that their fatigue and sleep quality levels would be monitored for four weeks without any intervention (other than routine treatment given by the physician). Patients in this group were asked to fill out the Fatigue Severity Scale and the Richard-Campbell Sleep Scale at the beginning and again in the 4th week.
No interventions assigned to this group
Interventions
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acupressure application
The patients in the experimental group received acupressure application for a total of 8 sessions, 2 sessions per week.
Eligibility Criteria
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Inclusion Criteria
* Those who can read and write,
* Those who can speak Turkish,
* Patients diagnosed with multiple sclerosis,
* Patients who do not have a neurological disease other than MS,
* Those who volunteer to participate in our study,
* Patients who are conscious and do not have a psychiatric health problem
Exclusion Criteria
* Patients with bleeding problems, pacemaker or heart failure and a diagnosed condition, mass and flattening in the neck,
* Patients with a diagnosis other than MS (such as subarachnoid hemorrhage, aneurysm, dementia, a psychiatric disease),
* Patients who have had a hemorrhagic stroke,
* Patients with malignancy,
* Patients with vision and hearing problems,
* Patients who do not volunteer to participate in our study
18 Years
65 Years
ALL
No
Sponsors
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Yuzuncu Yıl University
OTHER
Responsible Party
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Gülden Atan
Assistant Professor
Principal Investigators
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Gülden Atan, PHD
Role: PRINCIPAL_INVESTIGATOR
Faculty of health science, Yuzuncu Yıl University , Van, TURKEY.
Locations
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Yuzuncu Yıl University , Faculty of health science
Van, , Turkey (Türkiye)
Countries
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Other Identifiers
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MS-GULDEN
Identifier Type: -
Identifier Source: org_study_id
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