NCT07118553

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
27

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 14, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 5, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 12, 2025

Completed
Last Updated

August 12, 2025

Status Verified

August 1, 2025

Enrollment Period

1 month

First QC Date

August 5, 2025

Last Update Submit

August 5, 2025

Conditions

Keywords

premenstrual syndromefacemassagequality of life

Outcome Measures

Primary Outcomes (1)

  • Visual Analogue Scale (VAS)

    The VAS was used to assess participants' pain intensity. The VAS is a scale ranging from 0 ('No pain') to 10 points ('Unbearable pain') on a horizontal line. According to the VAS, '0' means no pain, while 10 points means severe pain.

    six weeks

Secondary Outcomes (3)

  • Perceived Stress Scale (PSS)

    six weeks

  • Short Form-12

    six weeks

  • Profile of Mood States (POMS):

    six weeks

Study Arms (2)

Facial massage group

EXPERIMENTAL

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.

Other: classic facial massage

control group

NO INTERVENTION

The control group received no intervention. Participants continued their daily routines as usual.

Interventions

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

Facial massage group

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Trabzon Unversity

Trabzon, Tonya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Premenstrual SyndromeFacies

Condition Hierarchy (Ancestors)

Menstruation DisturbancesPathologic ProcessesPathological Conditions, Signs and SymptomsDisease Attributes

Study Officials

  • Aysun Yağci Şentürk, Ph.D

    Trabzon University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
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.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: two groups (intervention and control groups)
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

August 5, 2025

First Posted

August 12, 2025

Study Start

May 14, 2025

Primary Completion

June 20, 2025

Study Completion

June 20, 2025

Last Updated

August 12, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations