Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
ID07397429

Group Therapy Using the I-Reconstruction Psychotherapy Method for Reducing Anxiety Levels: a Randomized Controlled Trial

Led by International Association Psychosomatics And Health Therapy · Updated on 2026-02-09

36

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether the group therapy method called "I-Reconstruction" can help reduce anxiety levels in adults. The study targets individuals with clinically significant anxiety and investigates if emotional stability improves after the therapy. Researchers will compare participants who attend the therapy sessions with those receiving usual care to determine if the new method offers more lasting benefits. The study involves three groups: two experimental groups receiving the "I-Reconstruction" therapy and one control group continuing usual care without intervention. Participants in the therapy groups will attend ten weekly online group sessions, each lasting two hours, led by certified therapists. The therapy focuses on addressing preverbal trauma and internal conflicts related to desire, possession, and satisfaction through psychoeducation, emotional exploration, and group reflection. Participants will be involved in a 17-month process including screening, therapy sessions, and follow-up assessments at 3, 6, and 12 months after completing the therapy. They will complete questionnaires measuring anxiety, depression, internal conflicts, and preverbal dysregulation at multiple time points. The main outcomes include changes in anxiety levels assessed by the Beck Anxiety Inventory and Hospital Anxiety and Depression Scale. The control group will undergo the same assessments without receiving the therapy.

CONDITIONS

Brief Title

Group Therapy Using the "I-Reconstruction" Psychotherapy Method to Reduce Anxiety Levels

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 55 years (inclusive)
  • Clinically significant anxiety with Beck Anxiety Inventory score of 9 or higher
  • Anxiety subscale score on Hospital Anxiety and Depression Scale (HADS-A) of 11 or higher
  • Significant preverbal trauma with a total score of 16 or more on the Diagnostics of Preverbal Dysregulation questionnaire
  • Specific scores of 5 or higher on Desire and Satisfaction subscales and 6 or higher on Possession (Obsession) subscale of the DPD
  • Presence of internal conflicts with a score of 1 or more on the Internal Conflict Test skin tissue measurement scale
  • Willingness to follow the study protocol and participate in online therapy sessions
Not Eligible

You will not qualify if you...

  • Current participation in any psychotherapy
  • Use of psychotropic medications within the last 30 days
  • Diagnosed severe mental disorders requiring specialized psychiatric care or inpatient treatment
  • Presence of acute suicidal risk
  • Substance abuse including alcoholism and drug addiction
  • Not meeting the specific threshold values for inclusion criteria

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (online questionnaire)

Treatment

Duration - 10 weeks

Participants attend ten weekly online group therapy sessions based on the I-Reconstruction psychotherapy method to reduce anxiety levels.

Weekly online group therapy sessions

Follow-up

Duration - Up to 12 months after treatment

Participants complete a series of assessments to monitor anxiety and psychological outcomes at 3, 6, and 12 months after the intervention.

3 assessment visits at 3, 6, and 12 months post-intervention

Trial Site Locations

Total: 1 location

1

International Association of Psychosomatics and Body Therapy

Kyiv, Kyiv Oblast, Ukraine, 03057

Actively Recruiting

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Research Team

T

Tetiana Pavlenko

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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