Recruiting

Islamic-Oriented vs. Standard Ericksonian Hypnotherapy for Anxiety and Depression

This randomized controlled trial (RCT) aims to compare the effectiveness of Islamic-Oriented Ericksonian Hypnotherapy (IEH) and Standard Ericksonian Hypnotherapy (SEH) in reducing symptoms of anxiety and depression. The study will enroll 90 participants with mild to moderate anxiety and depression, who will be randomly assigned to one of three groups: (1) IEH intervention, (2) SEH intervention, or (3) control group (no intervention). Participants in the intervention groups will receive 12 weekly hypnotherapy…

ClinicalTrials.gov IDNCT06844058
PhaseNA
Enrollment90
SponsorIstanbul Nisantasi University
Age18 Years
SexALL
I'm interested View official listing

Conditions studied

Anxiety Disorders, Depressive Disorder

About this study

This randomized controlled trial (RCT) aims to compare the effectiveness of Islamic-Oriented Ericksonian Hypnotherapy (IEH) and Standard Ericksonian Hypnotherapy (SEH) in reducing symptoms of anxiety and depression. The study will enroll 90 participants with mild to moderate anxiety and depression, who will be randomly assigned to one of three groups: (1) IEH intervention, (2) SEH intervention, or (3) control group (no intervention). Participants in the intervention groups will receive 12 weekly hypnotherapy sessions, each lasting 60 minutes. The primary outcomes include changes in Beck Depression Inventory-II (BDI-II) and Beck Anxiety Inventory (BAI) scores from baseline to post-intervention and at a 4-week follow-up. The study will also assess whether religious belief levels moderate the effects of the intervention using the OK-Religious Attitude Scale. Data collection will be performed at Istanbul Nişantaşı University, and ethical approval has been obtained.

Interventions

Primary outcomes

Eligibility information

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.

Study locations

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.