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RecruitingNCT06844058IEH-RTCUpdated Mar 26, 2025

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

An interventional study of Islamic-Oriented Ericksonian Hypnotherapy (IEH) and Standard Ericksonian Hypnotherapy (SEH) in Anxiety Disorders and Depressive Disorder, sponsored by Istanbul Nisantasi University. Recruiting at 1 site in Turkey. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-26.

Sponsored by Istanbul Nisantasi University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as recruiting.
  • Started Jan 2025; still recruiting 1 year 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

Read the detailed description

This randomized controlled trial evaluates the differential effects of Islamic-Oriented Ericksonian Hypnotherapy (IEH) and Standard Ericksonian Hypnotherapy (SEH) in alleviating symptoms of anxiety and depression among religious Muslim adults. The primary objective is to examine whether the integration of Islamic religious elements into Ericksonian hypnotherapy enhances clinical outcomes compared to its standard application.

The study follows a parallel-group design with three arms: IEH, SEH, and a no-intervention control. Ninety participants (30 per group) are randomized using stratified block randomization based on age and gender. All intervention sessions are manualized, delivered by trained clinical psychologists, and conducted weekly over 12 weeks (each lasting 60 minutes).

IEH sessions incorporate culturally and religiously adapted therapeutic elements, such as Quranic metaphors, Islamic imagery, and spiritual affirmations, in line with the Ericksonian framework. SEH sessions utilize traditional hypnotic techniques including metaphorical storytelling, guided imagery, and indirect suggestions, without religious content.

Primary outcome measures include changes in Beck Depression Inventory-II (BDI-II) and Beck Anxiety Inventory (BAI) scores from baseline to Week 12 (post-intervention) and Week 16 (follow-up). Secondary analyses will investigate whether religiosity levels (measured via the OK-Religious Attitude Scale) moderate treatment effects. Blinded outcome assessors will ensure unbiased data collection.

This study addresses the need for culturally responsive mental health interventions within Muslim populations. Ethical approval was obtained from the İstanbul Nişantaşı University Ethics Committee (Approval No: 20250103-27). Results are expected to contribute to evidence-based development of spiritually integrated psychotherapeutic models for anxiety and depression.

02

Conditions studied

  • Anxiety Disorders
  • Depressive Disorder

Keywords

  • Hypnotherapy
  • Ericksonian Hypnosis
  • Islamic Psychology
  • Anxiety Reduction
  • Depression Treatment
  • Culturally Adapted Psychotherapy
  • Religious-Based Therapy
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's planned enrollment of 90 is close to the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Istanbul Nisantasi University is the lead sponsor of 20 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Islamic-Oriented Ericksonian Hypnotherapy (IEH) Group

    Participants 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.

    Behavioral: Islamic-Oriented Ericksonian Hypnotherapy (IEH)

  • Active comparator
    Standard Ericksonian Hypnotherapy (SEH) Group

    Participants 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.

    Behavioral: Standard Ericksonian Hypnotherapy (SEH)

  • No intervention
    Control Group (No Intervention)

    Participants do not receive any intervention but will complete assessments at baseline, post-intervention (Week 12), and follow-up (Week 16).

Interventions

  • BehavioralIslamic-Oriented Ericksonian Hypnotherapy (IEH)

    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.

  • BehavioralStandard Ericksonian Hypnotherapy (SEH)

    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.

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: Baseline, Week 12 (post-intervention), Week 16 (follow-up)

  2. 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.

    Time frame: Baseline, Week 12, Week 16

07

Study locations

1 of 1 sites recruiting
  • İstanbul Nişantaşı University
    İstanbul, 34277, Turkey
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — 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.

Supporting information: Study protocol, Sap, Csr

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 26, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06844058
Lead sponsor
Istanbul Nisantasi University
Responsible party
Metin Çınaroğlu (Principal Investigator, Istanbul Nisantasi University) — Principal investigator
First posted
Feb 25, 2025
Start date
Jan 15, 2025
Primary completion
Jun 25, 2025 (estimated)
Completion
Aug 15, 2025 (estimated)
Last update
Mar 26, 2025

Study contacts

Metin Çınaroğlu, Phd
Contact
metin.cinaroglu@nisantasi.edu.tr
+905324732070
Gözde Mert, Phd
Contact
gozde.mert@nisantasi.edu.tr
+905359403399
Metin Çınaroğlu, Phd
principal investigator · Istanbul Nisantasi Universitesi

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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