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NCT Number: NCT06811311

EEG Study on Neurophysiological and Psychological Effects of Ericksonian Hypnotherapy in Generalized Anxiety Disorder

This study examines the neurophysiological and psychological effects of Ericksonian hypnotherapy in individuals diagnosed with Generalized Anxiety Disorder (GAD). Using electroencephalography (EEG), the study aims to assess changes in brain activity and anxiety symptoms before and after treatment.

A total of 60 participants will be recruited from both governmental and private psychiatric clinics in Istanbul. Participants will be randomly assigned to either the intervention group (receiving 12 Ericksonian hypnotherapy sessions over 12 weeks) or the control group (receiving no intervention).

The primary outcome measures include changes in EEG patterns, specifically alpha, theta, and frontal asymmetry indices, and changes in anxiety severity, measured by the Beck Anxiety Inventory (BAI), Generalized Anxiety Disorder-7 (GAD-7), and State-Trait Anxiety Inventory (STAI). Secondary measures include emotional regulation (DERS) and quality of life (WHOQOL-BREF).

This study aims to provide scientific evidence on the effectiveness of Ericksonian hypnotherapy as a complementary treatment for GAD and its impact on brain function and emotional well-being.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Üsküdar University, Neuro-Psychology Lab

Istanbul, 34277, Turkey (Türkiye)

Location status: Recruiting

Location contact

Metin Çınaroğlu, Phd

CONTACT

[email protected]

09053247320

Metin Çınaroğlu, Phd

SUB_INVESTIGATOR

Selami Varol Ülker, Phd

CONTACT

[email protected]

+905364360941

Selami Varol Ülker, Phd

PRINCIPAL_INVESTIGATOR

About this study

This study investigates the neurophysiological and psychological effects of Ericksonian hypnotherapy in individuals diagnosed with Generalized Anxiety Disorder (GAD) using electroencephalography (EEG). The research aims to determine whether Ericksonian hypnotherapy produces measurable changes in brain activity and anxiety symptoms.

A total of 60 participants (30 per group) will be recruited from both governmental and private psychiatric clinics in Istanbul. Participants will be diagnosed with GAD based on DSM-5 criteria and will undergo structured psychiatric evaluation before inclusion.

Study Design Intervention Group (n = 30): Participants will receive 12 individual Ericksonian hypnotherapy sessions, each lasting 90 minutes, delivered over 12 weeks. The hypnotherapy protocol will include permissive language, metaphorical storytelling, and indirect suggestions tailored to anxiety-related cognitive and emotional patterns.

Control Group (n = 30): Participants will receive no psychological intervention during the study period.

Both groups will undergo baseline and post-intervention EEG measurements and complete psychological assessments.

Primary Outcome Measures:

EEG Changes: Resting-state and task-based EEG recordings will be analyzed for alpha, theta power, frontal asymmetry indices, and event-related potentials (ERPs: P300, N200) to assess neurophysiological effects of hypnotherapy.

Anxiety Severity: Beck Anxiety Inventory (BAI), Generalized Anxiety Disorder-7 (GAD-7), and State-Trait Anxiety Inventory (STAI) will be used to measure anxiety symptom changes.

Secondary Outcome Measures:

Emotional Regulation: Measured using the Difficulties in Emotion Regulation Scale (DERS).

Quality of Life: Evaluated with the World Health Organization Quality of Life Scale (WHOQOL-BREF).

Timeline:

Recruitment Period: February 1, 2025 - March 15, 2025 Baseline Assessments: March 2025 Intervention Period: April 1, 2025 - June 2025 Post-Intervention Assessments: July 2025 This study aims to provide scientific evidence on the efficacy of Ericksonian hypnotherapy as a complementary treatment for Generalized Anxiety Disorder by evaluating both neurophysiological and psychological changes. Findings may contribute to the development of alternative therapeutic approaches for anxiety disorders.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of Generalized Anxiety Disorder (GAD) based on DSM-5 criteria
  • Aged 18-65 years
  • Capable of providing written informed consent
  • Fluent in Turkish (for hypnosis and assessments)
  • Not currently receiving psychotherapy or pharmacological treatment for anxiety

Exclusion criteria

  • Presence of comorbid psychiatric disorders (e.g., schizophrenia, bipolar disorder, major depression requiring immediate intervention)
  • History of neurological conditions (e.g., epilepsy, traumatic brain injury, stroke)
  • Current use of medications affecting EEG activity (e.g., benzodiazepines, SSRIs, antipsychotics)
  • Previous experience with hypnotherapy (to avoid expectancy bias)
  • Substance abuse or dependence within the last six months
  • Pregnancy or breastfeeding
  • Severe medical conditions that may interfere with participation

Treatment and study plan

Ericksonian Hypnotherapy

Behavioral

Ericksonian hypnotherapy is a therapeutic approach that utilizes indirect suggestion, storytelling, and metaphorical language to induce a trance state and facilitate psychological change. This intervention aims to reduce anxiety symptoms, improve emotional regulation, and alter neurophysiological responses as measured by EEG. Participants will undergo 12 individual sessions, each lasting 90 minutes, over a period of 12 weeks.

Primary outcomes

  1. EEG Changes in Brain Activity

    Time frame: Baseline (Pre-intervention) and Post-intervention (12 weeks)

    Measure: Changes in alpha, theta power, and frontal asymmetry indices before and after intervention Description: EEG will be used to assess changes in resting-state brain activity and event-related potentials (ERPs: P300, N200), evaluating neurophysiological effects of Ericksonian hypnotherapy.

  2. Beck Anxiety Inventory (BAI)

    Time frame: Baseline and Post-intervention (12 weeks)

    Change in BAI scores (0-63, higher scores indicate more severe anxiety).

Secondary outcomes

  1. Generalized Anxiety Severity (Generalized Anxiety Disorder-7, GAD-7)

    Time frame: Baseline and Post-intervention (12 weeks)

    Change in GAD-7 scores (0-21, higher scores indicate more severe anxiety)

  2. State and Trait Anxiety Levels (State-Trait Anxiety Inventory, STAI)

    Time frame: Baseline and Post-intervention (12 weeks)

    Change in STAI scores (20-80, higher scores indicate greater anxiety).

  3. Difficulties in Emotion Regulation Scale, (DERS)

    Time frame: Baseline and Post-intervention (12 weeks)

    Change in DERS scores (36-180, higher scores indicate greater emotion regulation difficulties).

  4. World Health Organization Quality of Life Scale, (WHOQOL-BREF)

    Time frame: Baseline and Post-intervention (12 weeks)

    Change in WHOQOL-BREF scores (0-100, higher scores indicate better quality of life).

Study contacts

Contact information is provided by the study sponsor or research team.

Metin Çınaroğlu, Phd

CONTACT

[email protected]

+90532-473-20-70

Selami Varol Ülker, Phd

CONTACT

[email protected]

+90536-436-09-41

Sponsors and collaborators

Lead sponsor

Uskudar University

Other

Collaborators

  • Beykoz University
  • Istanbul Nisantasi University

Registry information

Official study title

Neurophysiological and Psychological Effects of Ericksonian Hypnotherapy on Generalized Anxiety Disorder: An EEG-Based Clinical Study

Acronym: EEG-HypnoGAD

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 6, 2025
Registry last updated
Feb 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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