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 — BEHAVIORAL
    The 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 Group
    Participants 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 Group
    Participants 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

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