Theta Healing-Based Intervention in Women With Polycystic Ovary Syndrome
- Sponsor
- Ankara Medipol University
- Study ID
- NCT07630441
- Status
- Not Yet Recruiting
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Conditions
- Infertility
- Polycystic Ovarian Syndrome (PCOS)
- Psychological Stress
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 45 Years
- Healthy Volunteers
- Not accepted
Interventions
- Theta Healing-Based Intervention — BEHAVIORALThe intervention consists of a structured 5-day Theta Healing-based online program including guided meditation, relaxation exercises, visualization, positive affirmations, subconscious awareness practices, and self-compassion-focused exercises. Audio recordings will be delivered daily via WhatsApp, and a final online group session will be conducted on the fifth day by a certified Theta Healing practitioner.
Study Details
This randomized controlled study aims to evaluate the effect of a Theta Healing-based intervention on fertility concerns, self-compassion, and body image in women diagnosed with Polycystic Ovary Syndrome (PCOS). Participants will be randomly assigned to intervention and control groups. The intervention group will receive a structured 5-day Theta Healing-based online intervention program, while the control group will continue routine care. Outcome measures will be assessed at baseline and 6 weeks after the intervention.
Key Dates
- First listed
- Jun 5, 2026
- Start date
- Jun 8, 2026
- Status verified
- Jun 2026
- Primary completion
- Jul 24, 2026
- Completion
- Sep 15, 2026
Study Design
- Enrollment
- 142 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Theta Healing Intervention GroupParticipants in this group will receive a structured Theta Healing-based intervention program including guided meditation, subconscious belief transformation, positive cognition development, relaxation exercises, and awareness practices.
- No Intervention: Control GroupParticipants in this group will not receive any intervention and will continue their usual daily routines throughout the study period.
Primary Outcome Measure
Fertility Anxiety Score [ Time Frame: Baseline and 6 weeks after intervention ]
Central Contacts
- Tugba Tahta, Assistant Professor+905425085543
- Seniha Balci Cebeci, Research Assistant+905439132414
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