Clinical trial · Interventional
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
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Infertility | — | UNRESOLVED | — |
| Polycystic Ovarian Syndrome (PCOS) | — | UNRESOLVED | — |
| Psychological Stress | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Theta Healing-Based Intervention | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Theta Healing Intervention Group
- description
- 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.
- interventionNames
- Behavioral: Theta Healing-Based Intervention
- type
- NO_INTERVENTION
- label
- Control Group
- description
- Participants in this group will not receive any intervention and will continue their usual daily routines throughout the study period.
Primary outcomes (1)
- measure
- Fertility Anxiety Score
- timeFrame
- Baseline and 6 weeks after intervention
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 45 Years
Show eligibility criteria text
Inclusion Criteria: * 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 Exclusion Criteria: * Diagnosed psychiatric disorder * Participation in another psychological intervention program * Any health condition preventing participation in the intervention sessions * Incomplete questionnaire responses
References
Publications (0)
Data not yet available