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

NCT07397429 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2026-02-09

No results posted yet for this study

Summary

Brief Summary of the Study The aim of this clinical trial is to find out if the group therapy method "Self-Reconstruction" helps to reduce anxiety in adults. The researchers want to see if the participants' emotional state becomes more stable after completing the course.

The main questions that this study aims to answer are:

Do people's anxiety levels decrease after taking the course of "I-Reconstruction" classes?

Do the positive effects of the classes persist 3, 6 and 12 months after they finish?

Do the participants' quality of life and ability to enjoy life improve?

The researchers will compare a group of people who attend the therapy classes with a group of people who receive usual care to see if the new method is more effective.

Participants will:

Participate in 10 online group meetings once a week.

Do simple breathing and movement exercises to calm the body and emotions.

Discuss your feelings and desires with a professional in a safe group.

Complete questionnaires about your condition at the beginning, during, and after the study.

Conditions

Interventions

DRUG

Experimental: Active "I-Reconstruction" Therapy

The intervention consisted of a structured group psychotherapy program based on the "l-Reconstruction" method. The program included ten weekly group sessions, each lasting 120 minutes, delivered online by a certified therapist trained in the method. The intervention targeted anxiety through therapeutic work with preverbal trauma and internal conflicts by reconstructing core personality components related to desire, ownership, and the capacity for pleasure. The therapeutic process combined psychoeducation, analysis of preverbal acts, exploration of emotional and bodily responses, reconstruction of traumatic experiential patterns, and structured group reflection and integration. The intervention followed a standardized protocol to ensure consistency across groups and therapists.

DRUG

Standard Care (Treatment as Usual)

Participants assigned to the control group did not receive any structured psychotherapeutic intervention as part of the study. During the intervention period, no active treatment, group sessions, or therapeutic procedures were provided by the research team. The control condition was designed to serve as a non-intervention comparison group for evaluating the effects of the "l-Reconstruction" group psychotherapy.

Sponsors & Collaborators

  • International Association Psychosomatics And Health Therapy

    lead OTHER

Principal Investigators

  • Tetiana Pavlenko · International Association of Psychosomatics and Health Therapy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-02
Primary Completion
2027-05-02
Completion
2027-06-30

Countries

  • Ukraine

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07397429 on ClinicalTrials.gov