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Clinical Trials/NCT04838691
NCT04838691CompletedNot Applicable

The Effect of Interpersonal Counseling in Symptoms Management of Premenstrual Syndrome

Istanbul University - Cerrahpasa (IUC)1 site in 1 country80 target enrollmentStarted: April 6, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
Premenstrual Symptom Screening Tool

Study Overview

Brief Summary

This study aims to test the effectiveness of interpersonal counseling in PMS symptom management in university students experiencing PMS symptoms.

Detailed Description

People diagnosed with Premestrual Syndrome were identified through an online questionnaire. 80 people who were identified and accepted to study were divided into two groups as experiment and control. Initially, pre-menstrual screening tool, interpersonal relationship dimensions scale and perceived stress scale were applied to all groups. Then, 8 sessions of interpersonal counseling, each lasting 40 minutes, were applied to the experimental group for 2 months. Scales were repeated for both groups after the application was completed. Repeated measurements were made 3 months later.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •According to the Pre-menstrual Symptom Screening Instrument, which is located in the group living with AES (Pre-Mental Syndrome)
  • •between the ages of 18-30
  • •Menstruating at regular intervals for at least 2 years (21-35 days)
  • •Those who have never given birth
  • •Speak and understand Turkish
  • •It will consist of people who have not received antidepressant, oral contraceptive or hormone therapy for any reason.

Exclusion Criteria

  • •Having a known gynecological disease (endometriosis, polycystic ovary, ...)
  • •A known, ongoing physical health problem (diabetes, rheumatic disease, ...)
  • •Any psychiatric disease diagnosed (psychotic disorder, mood disorder, anxiety disorder ...)
  • •People who use cigarettes, alcohol or substances

Arms & Interventions

interpersonal relations counseling applied

Experimental

8 sessions of interpersonal relations counseling, each lasting 40 minutes, were applied for 2.

Intervention: interpersonal counseling (Behavioral)

no application

No Intervention

No action taken.

Outcomes

Primary Outcomes

Premenstrual Symptom Screening Tool

Time Frame: Baseline (beginning), Change from Baseline PMDD or PMS after 2 months, Change from Baseline PMDD or PMS after 5 months,

Women will be divided into 3 different groups as a result of the points they get from PSST. The first group will consist of women who fully meet the PMDD criteria. These Women must have at least one of the four main symptom groups from the group A symptoms plus any of the 4 symptoms marked as moderate to severe on the instrument. In addition, he should have reported that at least one of the questions in group B was severe, and yes answers should be given to both questions in group C.The second group is the group that meets the PMS living criteria. These women are expected to have marked at least one of the 4 main symptoms as moderate to severe from the group A questions and any other 4 symptoms as moderate to severe to answer the group B questions as moderate to severe, and to answer yes to at least one question from the C group.The third group will be considered as the group with subthreshold symptoms consisting of those who do not meet the criteria for entering the other two groups.

Secondary Outcomes

  • Scale Of Interpersonal Relatıonshıps Dımensıons(Baseline (beginning), Change from Baseline Sub-dimensions of Interpersonal Relationships Scale after 2 months, Change from Baseline Sub-dimensions of Interpersonal Relationships Scale after 5 months)
  • Perceived stress scale(Baseline (beginning), 2 months after beginning, 3 months after beginning)

Investigators

Sponsor
Istanbul University - Cerrahpasa (IUC)
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Zeynep Seyyide Bozkurt

Principle Investigator

Istanbul University - Cerrahpasa (IUC)

Study Sites (1)

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