NCT06704399

Brief Summary

The aim of this study is to manage individual psychoeducation in acceptance and commitment therapy for problems with panic disorder and to evaluate the effect of this program on rumination and self-resilience.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
13mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress37%
Sep 2025Jun 2027

First Submitted

Initial submission to the registry

November 21, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 26, 2024

Completed
10 months until next milestone

Study Start

First participant enrolled

September 30, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2027

Last Updated

May 8, 2025

Status Verified

May 1, 2025

Enrollment Period

1 year

First QC Date

November 21, 2024

Last Update Submit

May 7, 2025

Conditions

Keywords

ruminationself-compassion

Outcome Measures

Primary Outcomes (1)

  • Ruminative Thought Style Questionnaire

    The scale is a 7-point Likert type consisting of 20 items. 7 = Very good and 1 = Not at all, and participants are asked to score each item according to how much it reflects themselves. The internal consistency coefficient of the scale, Cronbach's alpha value, was found to be .907. In the item analysis, the item total score correlation was calculated and the total correlations of the items were found to be between 0.474 and 0.699.

    7 week

Secondary Outcomes (1)

  • Self Compassion Scale

    7 week

Study Arms (2)

psycoeducation

ACTIVE COMPARATOR

Psychoeducation based on acceptance and commitment therapy will be applied to the experimental group of 25 people. Pre-test, post-test and follow-up test will be applied.

Other: Acceptance and Commitment Therapy-Based Psychoeducation

control

ACTIVE COMPARATOR

No intervention will be applied to the control group of 25 people. Pre-test, post-test and follow-up test will be applied.

Interventions

Psychoeducation based on acceptance and commitment therapy will be applied to the experimental group.

psycoeducation

No intervention will be applied to the control group.

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients diagnosed with Panic Disorder followed in Muğla Training and
  • Research Hospital Psychiatry Polyclinics,
  • Those between the ages of 18-65 who agree to participate in the research,
  • Those who were in a euthymic mood during the interview, according to physician control,
  • Those who speak Turkish,
  • Those who are literate,
  • Those who have a computer and internet access for the program to be conducted online if deemed necessary during the research process,

You may not qualify if:

  • Having a diagnosis of a psychiatric disease in addition to panic disorder,
  • Having an attack period during the training period,

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mugla Sıtkı Koçman University

Muğla, mentese, 48000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Panic DisorderRumination Syndrome

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Anxiety DisordersMental DisordersGastrointestinal DiseasesDigestive System DiseasesFeeding and Eating Disorders

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Central Study Contacts

Fatmanur OZCAN MIRCALI

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Two groups included experimental and control group, pre-test, post-test and follow-up test.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator, PhD student

Study Record Dates

First Submitted

November 21, 2024

First Posted

November 26, 2024

Study Start

September 30, 2025

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

June 30, 2027

Last Updated

May 8, 2025

Record last verified: 2025-05

Locations