Factors Affecting Premenstrual Syndrome

NCT ID: NCT07118553

Last Updated: 2025-08-12

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-14

Study Completion Date

2025-06-20

Brief Summary

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Premenstrual pain syndrome is a common problem that affects many women of reproductive age. In this study, we aimed to determine whether facial massage would improve the quality of life, mood, pain and stress levels of women with premenstrual syndrome.

Detailed Description

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Young women over the age of 18 with premenstrual syndrome were randomly divided into two groups. One group received facial massage for six weeks, while the other group received no intervention. At the end of six weeks, pain, stress, quality of life and mood were assessed in both groups.

Conditions

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Premenstrual Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

two groups (intervention and control groups)
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
The intervention group received facial massage. The control group continued their lives in the same manner. At the end of six weeks, the researchers completed post-tests for both groups.

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.

Group Type EXPERIMENTAL

classic facial massage

Intervention Type OTHER

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.

Group Type NO_INTERVENTION

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* at least 111 points or more on the Premenstrual Syndrome Scale
* 8 years of age or older
* to be volunteer for the study

Exclusion Criteria

* presence of any open wounds, allergies, etc. that would prevent facial massage
* the presence of routinely used gynaecological medication
* regular exercise
* unwillingness to participate
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Trabzon University

OTHER

Sponsor Role lead

Responsible Party

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Aysun YAĞCİ ŞENTÜRK

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

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)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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TU-TMYO-AYŞ-01

Identifier Type: -

Identifier Source: org_study_id

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