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
49 participants
INTERVENTIONAL
2022-02-01
2022-09-05
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
SINGLE
Study Groups
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Experimental group
In the hand area, firstly, the points will be determined by means of the diagnostic stick and massage will be applied with buckwheat seeds. This massage will be 3 sessions a week, and a total of 6 sessions in 2 weeks.
sujok therapy
sujok therapy
control group
A questionnaire will be applied to the patients by the researcher. Questionnaires will be made as pre-test and post-test.
No interventions assigned to this group
Interventions
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sujok therapy
sujok therapy
Eligibility Criteria
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Inclusion Criteria
* Fatigue Severity Measurement - Visual Analogue Scale (VAS) fatigue score of 3 and above,
* Pain Severity Measurement - Visual Analogue Scale (VAS) pain score of 3 and above,
* Measurement of Nausea and Vomiting Severity - Patients with a Visual Analogue Scale (VAS) nausea and vomiting score of 3 and above will be included.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Ataturk University
OTHER
Responsible Party
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Demet GUNES
Principal Investigator
Locations
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Atatürk Universty
Erzurum, , Turkey (Türkiye)
Countries
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Other Identifiers
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Demettez
Identifier Type: -
Identifier Source: org_study_id
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