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NCT07630441Not yet recruiting

Theta Healing-Based Intervention in Women With Polycystic Ovary Syndrome

The Effect of a Theta Healing-Based Intervention on Fertility Anxiety, Body Self-Compassion, and Body Image in Women Diagnosed With Polycystic Ovary Syndrome: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 5 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
142 (estimated)
First submitted
25 May 2026
Start date
8 Jun 2026
Primary completion date
24 Jul 2026
Lead sponsor
Ankara Medipol University
NCT number
NCT07630441

What you commit to

  • Study type: Interventional
  • Planned participants: 142
  • From 8 Jun 2026 to the primary completion date, 24 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Diagnosed psychiatric disorder
  • Any health condition preventing participation in the intervention sessions

Other

  • Participation in another psychological intervention program
  • Incomplete questionnaire responses

Who the study is looking for

  • Women aged 18-45 years
  • Diagnosed with Polycystic Ovary Syndrome (PCOS)
  • Able to read and understand Turkish
  • Voluntary participation in the study
  • Access to a smartphone and internet connection

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ankara Medipol University Faculty of Health Sciences
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.