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
27 participants
INTERVENTIONAL
2025-05-14
2025-06-20
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
TREATMENT
SINGLE
Study Groups
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Facial massage group
Classical facial massage was applied to the intervention group 2 days a week (with at least 1 day break) for 6 weeks. A session continued 20-30 minutes.
classic facial massage
Powder was used as an intermediate product in facial massage application. Before the application, the participants were made to lie in the supine position on the patient's bed. The researchers performed the facial massage by standing at the participants' bedside. During the massage application, three stroking movements were applied to the chin, mouth, nose, eyes and forehead areas, respectively. Kneading motion was then applied to the same areas three times each. Then, stroking was applied to these five areas again and the facial massage application was terminated at the end of approximately 20-30 minutes. Friction movement was applied to the temporal region in each stroking and kneading application
control group
The control group received no intervention. Participants continued their daily routines as usual.
No interventions assigned to this group
Interventions
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classic facial massage
Powder was used as an intermediate product in facial massage application. Before the application, the participants were made to lie in the supine position on the patient's bed. The researchers performed the facial massage by standing at the participants' bedside. During the massage application, three stroking movements were applied to the chin, mouth, nose, eyes and forehead areas, respectively. Kneading motion was then applied to the same areas three times each. Then, stroking was applied to these five areas again and the facial massage application was terminated at the end of approximately 20-30 minutes. Friction movement was applied to the temporal region in each stroking and kneading application
Eligibility Criteria
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Inclusion Criteria
* 8 years of age or older
* to be volunteer for the study
Exclusion Criteria
* the presence of routinely used gynaecological medication
* regular exercise
* unwillingness to participate
18 Years
40 Years
FEMALE
No
Sponsors
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Trabzon University
OTHER
Responsible Party
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Aysun YAĞCİ ŞENTÜRK
Assistant professor
Principal Investigators
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Aysun Yağci Şentürk, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Trabzon University
Locations
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Trabzon Unversity
Trabzon, Tonya, Turkey (Türkiye)
Countries
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Other Identifiers
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TU-TMYO-AYŞ-01
Identifier Type: -
Identifier Source: org_study_id
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