Islamic-Oriented vs. Standard Ericksonian Hypnotherapy for Anxiety and Depression
IEH-RTC
Efficacy of Islamic-Oriented Ericksonian Hypnotherapy vs. Standard Ericksonian Hypnotherapy in Reducing Anxiety and Depression: A Randomized Controlled Trial
1 other identifier
interventional
90
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 15, 2025
CompletedFirst Submitted
Initial submission to the registry
February 19, 2025
CompletedFirst Posted
Study publicly available on registry
February 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2025
CompletedMarch 26, 2025
March 1, 2025
5 months
February 19, 2025
March 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Beck Depression Inventory-II (BDI-II)
The study evaluates the effectiveness of Islamic-Oriented Ericksonian Hypnotherapy (IEH) vs. Standard Ericksonian Hypnotherapy (SEH) vs. No Intervention in reducing depressive symptoms. Depression severity will be assessed using the Beck Depression Inventory-II (BDI-II), comparing baseline, post-intervention (Week 12), and follow-up (Week 16) scores.
Baseline, Week 12 (post-intervention), Week 16 (follow-up)
Beck Anxiety Inventory (BAI)
The study measures reductions in anxiety symptoms among participants receiving IEH, SEH, or no intervention. Anxiety severity will be assessed using the Beck Anxiety Inventory (BAI), comparing scores from baseline to post-intervention and follow-up.
Baseline, Week 12, Week 16
Study Arms (3)
Islamic-Oriented Ericksonian Hypnotherapy (IEH) Group
EXPERIMENTALParticipants receive 12 weekly sessions of Islamic-Oriented Ericksonian Hypnotherapy (IEH), which integrates faith-based imagery, Quranic metaphors, and religiously adapted hypnotic suggestions alongside standard Ericksonian techniques. Each session lasts 60 minutes.
Standard Ericksonian Hypnotherapy (SEH) Group
ACTIVE COMPARATORParticipants receive 12 weekly sessions of Standard Ericksonian Hypnotherapy (SEH), using metaphorical storytelling, indirect suggestions, guided imagery, and hypnotic language patterns without religious integration. Each session lasts 60 minutes.
Control Group (No Intervention)
NO INTERVENTIONParticipants do not receive any intervention but will complete assessments at baseline, post-intervention (Week 12), and follow-up (Week 16).
Interventions
This intervention involves 12 weekly sessions (60 minutes each) of Ericksonian hypnotherapy integrated with Islamic religious elements. Sessions incorporate: Quranic metaphors and Islamic imagery Spiritual affirmations to enhance relaxation and emotional regulation Faith-based guided hypnosis adapted to cultural and religious beliefs Techniques such as indirect suggestions, therapeutic storytelling, and guided imagery The intervention is designed for Muslim participants with mild to moderate anxiety and depression.
Participants receive 12 weekly sessions (60 minutes each) of standard Ericksonian hypnotherapy, which includes: Metaphorical storytelling and guided imagery Indirect hypnotic suggestions to promote psychological flexibility Relaxation techniques to reduce anxiety and depressive symptoms Unlike the Islamic-Oriented Hypnotherapy (IEH), this intervention does not integrate religious or faith-based elements.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İstanbul Nişantaşı University
Istanbul, 34277, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Metin Çınaroğlu, Phd
Istanbul Nisantasi Universitesi
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 19, 2025
First Posted
February 25, 2025
Study Start
January 15, 2025
Primary Completion
June 25, 2025
Study Completion
August 15, 2025
Last Updated
March 26, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR
- Time Frame
- IPD and supporting information will be available after publication of study results and will remain accessible for five years post-publication.
- Access Criteria
- Researchers requesting access must submit a formal request specifying their intended use of the data. Access will be granted upon institutional review and approval by the research team. Requests can be made by contacting the corresponding author via email.
Deidentified individual participant data (IPD) will be shared upon publication of the study results in a peer-reviewed journal. The shared dataset will include anonymized scores from outcome measures (e.g., BDI-II, BAI) and will exclude any personally identifiable information. Data will be available upon reasonable request for research purposes.