NCT07202650 THE EFFECT OF GUİDED IMAGERY ON PREMENSTRUAL SYNDROME
| NCT ID | NCT07202650 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Baskent University |
| Condition | Guided Imagery |
| Study Type | INTERVENTIONAL |
| Enrollment | 48 participants |
| Start Date | 2026-05-15 |
| Primary Completion | 2026-09-20 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 48 participants in total. It began in 2026-05-15 with a primary completion date of 2026-09-20.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
EFFECT OF GUIDED IMAGERY ON PREMENSTRUAL SYNDROME IN UNIVERSITY STUDENTS Premenstrual Syndrome (PMS) is a condition characterized by physical, behavioral, and emotional symptoms that appear at the end of the luteal phase, 7-10 days before menstruation, and resolve with the onset of menstruation. Symptoms include irritability, loss of control, anxiety, depression, sleep disturbances, decreased concentration, unexplained crying, fatigue, weakness, changes in appetite, edema, headaches, joint and muscle pain, breast tenderness, altered sexual activity, and social withdrawal. In young women, PMS can negatively affect self-confidence, social relationships, quality of life, and academic performance. PMS treatment aims to relieve both physical and psychological symptoms and may include dietary supplements and complementary-alternative therapies. Approaches such as reflexology, pilates, acupressure, music, exercise, and guided imagery have shown promising results in reducing premenstrual symptoms. Mind-body-based approaches in complementary therapies are known to support psychological well-being. Guided imagery, a form of mind-body communication, involves the flow of thoughts and the way the mind encodes, stores, and expresses sensory information. It is based on the understanding that the mind and body are interconnected and that mental processes can influence physical responses. Guided imagery has been shown to reduce stress, improve mood, enhance sleep quality, strengthen the immune system, reduce fatigue, and minimize nausea and vomiting. Although effective, research on the use of guided imagery to reduce PMS symptoms in university students is limited. This study aims to investigate the effect of guided imagery on premenstrual syndrome in this population.
Eligibility Criteria
Inclusion Criteria: * Regular menstrual cycles (21-35 days over the last three cycles) * Age 18 years or older * No medical treatment for PMS * Ability to communicate effectively in Turkish * No psychiatric diagnosis or gynecological disorder (e.g., abnormal uterine bleeding, myoma, ovarian cysts) * A score \>89 on the Premenstrual Syndrome Scale (PMSS) * No prior participation in guided imagery training Exclusion Criteria: * Failure to perform guided imagery at the correct time or in the prescribed manner * Irregular menstruation during the last three months * Use of contraceptives * Use of analgesics during menstruation while participating in the study
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07202650 clinical trial?
This trial is open to female participants only, studying Guided Imagery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07202650 currently recruiting?
Yes, NCT07202650 is actively recruiting participants. Contact the research team at cansua05@gmail.com for enrollment information.
Where is the NCT07202650 trial being conducted?
This trial is being conducted at Ankara, Turkey (Türkiye).
Who is sponsoring the NCT07202650 clinical trial?
NCT07202650 is sponsored by Baskent University. The trial plans to enroll 48 participants.