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Premenstrual Syndrome and Interpersonal Counseling

NCT04838691 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2021-04-09

No results posted yet for this study

Summary

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

Conditions

  • Premenstrual Syndrome

Interventions

BEHAVIORAL

interpersonal counseling

In the intervention group, it will be administered for 40 minutes for 8 weeks to people with symptoms of premenstrual syndrome.

Sponsors & Collaborators

  • Istanbul University - Cerrahpasa

    lead OTHER

Principal Investigators

  • Neslihan Özcan, Professor · Istanbul University - Cerrahpasa

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-04-06
Primary Completion
2020-05-06
Completion
2020-08-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04838691 on ClinicalTrials.gov