Comparing Islamic and Standard Hypnotherapy for Anxiety and Depression

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial aims to evaluate the effectiveness of Islamic-Oriented Ericksonian Hypnotherapy (IEH) versus Standard Ericksonian Hypnotherapy (SEH) in reducing symptoms of anxiety and depression among Muslim adults. Ninety participants with mild to moderate anxiety and depression will be randomly assigned to one of three groups: IEH, SEH, or a control group with no intervention. Each intervention group will receive 12 weekly sessions of hypnotherapy, focusing on culturally and religiously adapted techniques for IEH and traditional methods for SEH. The study will measure changes in depression and anxiety scores using standardized inventories and assess the moderating effects of religious belief levels.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Muslim individuals aged 18-65 years.
* Mild to moderate anxiety and/or depression symptoms (assessed via Beck
* Depression Inventory-II (BDI-II) and Beck Anxiety Inventory (BAI)).
* No formal psychiatric diagnosis but experiencing psychological distress.
* High religious belief levels, assessed via OK-Religious Attitude Scale.
* Not currently receiving psychotherapy or psychotropic medication.
* Ability to give informed consent and complete the study requirements.

Exclusion Criteria:

* Severe psychiatric disorders (schizophrenia, bipolar disorder, severe MDD).
* Current use of psychotropic medication or undergoing psychotherapy.
* History of substance abuse or dependence.
* Diagnosed dissociative disorders (contraindications for hypnosis).
* Cognitive impairment affecting comprehension of intervention.
* Severe medical conditions that may interfere with participation.

Where it's running

• İstanbul Nişantaşı University
  Istanbul, Turkey (Türkiye) Recruiting

Study contacts

• Principal investigator: Metin Çınaroğlu, Phd — Istanbul Nisantasi Universitesi
• Study coordinator: Metin Çınaroğlu, Phd
• Email: metin.cinaroglu@nisantasi.edu.tr
• Phone: +905324732070

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.