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Clinical Trials/NCT01696578
NCT01696578
Completed
Not Applicable

Effectiveness of Combined Intervention Approaches in the Treatment of Affective Disorders and Chronic Pain in Victims of Torture and Massive Violence in Kosovo: A Randomized Controlled Trial

Rehabilitation and Research Centre for Torture Victims1 site in 1 country31 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PTSD
Sponsor
Rehabilitation and Research Centre for Torture Victims
Enrollment
31
Locations
1
Primary Endpoint
Change of anxiety symptom from baseline at 3 and 6 months
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This study will measure the effects of biofeedback supported cognitive behavioral therapy (BF-CBT) and group physiotherapy intervention in victims of torture and massive violence in Kosovo. The investigators aim to restore physical and psychosocial functioning of the victims of torture and massive violence with available rehabilitation practice and integrate them into the community. It is also our objective to build local knowledge and expertise to apply measurement principles and CBT methods in the Balkan region.

Detailed Description

The primary objective of this project is to contribute to the promotion of evidence-based health intervention which is dealing with the long-term consequences of trauma in the post-conflict Kosovo. This is the second phase of a series of multi-site case studies. Based on the knowledge generated in the first phase of project in 2007-2009, the investigators conclude that there is a need to continue with health interventions in northern Kosovo among those who are still suffering from the long-term effects of trauma. Many problems need to be addressed, ranging from unemployment and sleep disturbances to a high suicide rate. As our study shows, the situation is frequently complicated by co-morbidity between mental and physical problems, in particular, anger, hatred, severe depression and chronic pain. At this phase, the investigators aim to provide the available rehabilitation service to the victims of torture and massive violence in northern Kosovo. The investigators undertake an integrated intervention approach; that is a biofeedback supported cognitive-behavioral therapy (BF-CBT), which involves anger management, anxiety and phobia treatment (based on prolong exposure therapy)and a group physiotherapy intervention, which promotes physical fitness and social participation. The ultimate goal of this project is to determine both feasibility and the effectiveness of combined interventions in the countries with limited resources.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
April 2014
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Rehabilitation and Research Centre for Torture Victims
Responsible Party
Principal Investigator
Principal Investigator

Shr-Jie Wang

Principal investigator

Rehabilitation and Research Centre for Torture Victims

Eligibility Criteria

Inclusion Criteria

  • Victims of massive violence from northern Kosovo who reported one or more of the following experiences: 1) torture and other cruel, inhuman or degrading treatment or punishment (TCIDTP); 2) sexual harassment, molestation, rape or insertion of a blunt object into a genital organ and/or the rectum; 3) arrest and detention without warrant or order; or 4) extrajudicial execution of family members, perpetrated by members of law enforcement agency.
  • Clinical diagnosis of PTSD and one of following symptoms: depression, anxiety or chronic pain

Exclusion Criteria

  • With mental retardation or significant speech or cognitive impairment that would impede assessments
  • With past or present schizophrenia
  • With major alcoholic or substance abuse problems
  • Having recently undergone chemotherapy or chemo-radiotherapy for cancer or will have these therapy within following 6 months,
  • Having had any CBT in the past three years

Outcomes

Primary Outcomes

Change of anxiety symptom from baseline at 3 and 6 months

Time Frame: 0-3-6 months

Change of chronic pain symptom from baseline at 3 and 6 months

Time Frame: 0-3-6 months

Change of PTSD symptom from baseline at 3 and 6 months

Time Frame: 0-3-6 months

Change of depression symptom from baseline at 3 and 6 months

Time Frame: 0-3-6 months

Change of anger from baseline at 3 and 6 months

Time Frame: 0-3-6 months

Secondary Outcomes

  • Change of heart rate variability from baseline at 3 and 6 months(0-3-6 months)
  • Change of disability scale from baseline at 3 and 6 months(0-3-6 months)
  • Change of hand-grip strength from baseline at 3 and 6 months(0-3-6 months)
  • Change of standing balance from baseline at 3 and 6 months(0-3-6 months)
  • Change of BMI from baseline at 3 and 6 months(0-3-6 months)

Study Sites (1)

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