Effectiveness of Combined Intervention Approaches in the Treatment of Affective Disorders and Chronic Pain in War Victims

Sponsor
Rehabilitation and Research Centre for Torture Victims (Other)
Overall Status
Completed
CT.gov ID
NCT01696578
Collaborator
Kosova Rehabilitation Centre for Torture Victims (Other)
31
1
2
27
1.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: BF-CBT and group physiotherapy
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
31 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
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
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Dec 1, 2012
Actual Study Completion Date :
Apr 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: BF-CBT and group physiotherapy

Multivitamin+10 sessions of biofeedback supported cognitive behavioral therapy (BF-CBT) and 10 sessions of group physiotherapy

Behavioral: BF-CBT and group physiotherapy
Multivitamin+10 individual therapy sessions (BF-CBT) and 10 group therapy sessions (physical exercises) on a weekly basis

Active Comparator: Waiting list

The waiting list group receives only multivitamin pills while being waiting and will receive the same intervention 3 months later

Behavioral: BF-CBT and group physiotherapy
Multivitamin+10 individual therapy sessions (BF-CBT) and 10 group therapy sessions (physical exercises) on a weekly basis

Outcome Measures

Primary Outcome Measures

  1. Change of depression symptom from baseline at 3 and 6 months [0-3-6 months]

  2. Change of anxiety symptom from baseline at 3 and 6 months [0-3-6 months]

  3. Change of chronic pain symptom from baseline at 3 and 6 months [0-3-6 months]

  4. Change of anger from baseline at 3 and 6 months [0-3-6 months]

  5. Change of PTSD symptom from baseline at 3 and 6 months [0-3-6 months]

Secondary Outcome Measures

  1. Change of disability scale from baseline at 3 and 6 months [0-3-6 months]

  2. Change of hand-grip strength from baseline at 3 and 6 months [0-3-6 months]

  3. Change of standing balance from baseline at 3 and 6 months [0-3-6 months]

  4. Change of BMI from baseline at 3 and 6 months [0-3-6 months]

  5. Change of heart rate variability from baseline at 3 and 6 months [0-3-6 months]

Other Outcome Measures

  1. Change of reporting sleep disorder from baseline at 3 and 6 months [0-3-6 months]

  2. Change of reporting suicide ideation from baseline at 3 and 6 months [0-3-6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kosova Rehabilitation Centre for Torture Victims Pristina Kosovo 10000

Sponsors and Collaborators

  • Rehabilitation and Research Centre for Torture Victims
  • Kosova Rehabilitation Centre for Torture Victims

Investigators

  • Principal Investigator: Shr-Jie Wang, Ph.D., Rehabilitation and Research Centre for Torture Victims

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Shr-Jie Wang, Principal investigator, Rehabilitation and Research Centre for Torture Victims
ClinicalTrials.gov Identifier:
NCT01696578
Other Study ID Numbers:
  • RCTF5S2P4D1
First Posted:
Oct 1, 2012
Last Update Posted:
Apr 24, 2014
Last Verified:
Apr 1, 2014
Keywords provided by Shr-Jie Wang, Principal investigator, Rehabilitation and Research Centre for Torture Victims
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 24, 2014