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Completed

NCT Number: NCT03470779

Impact of Combined Psychotherapy and Physiotherapy Group Treatment Program for Survivors of Torture

The aim of this study is to assess the impact and feasibility of an interdisciplinary group treatment approach, involving psychotherapy and physiotherapy, with survivors of torture that are incarcerated in a prison in Kurdistan, Iraq. The primary aim is to develop initial estimates of treatment effects on symptoms and poor functioning consistent with centralized pain and post-traumatic stress disorder, anxiety, and/or depression. The secondary aim is to assess the feasibility of studying this interdisciplinary treatment program in which local Kurdish psychotherapists and physiotherapists provide a 10-week intervention in a prison, in the Kurdish Sorani language, and to Kurdish participants that present with mental health symptoms, physical complaints, and poor functioning

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Key information

Age range

18 year–100 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Sulaymaniyah Adult Male Reformatory

Sulaymaniyah, Kurdistan, Iraq

About this study

The aim of this randomized wait-list controlled pilot study is to assess the impact and feasibility of an interdisciplinary group treatment approach, involving psychotherapy and physiotherapy, with survivors of torture that are incarcerated in a prison in Kurdistan, Iraq. The primary aim is to develop initial estimates of treatment effects on symptoms and poor functioning consistent with centralized pain and post-traumatic stress disorder, anxiety, and/or depression. It is hypothesized that participants in the study will present with statistically significant improvements in some to all measures of symptoms and function. The secondary aim is to assess the feasibility of studying this interdisciplinary treatment program in which local Kurdish psychotherapists and physiotherapists provide a 10-week intervention in a prison, in the Kurdish Sorani language, and to Kurdish participants that present with mental health symptoms, physical complaints, and poor functioning

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age equal to or greater than 18 years
  • Incarcerated in the reformatory where research is conducted
  • Native speaker of Sorani, a Kurdish language
  • History of torture is reported and documented during the psychotherapy intake
  • Presents with symptoms consistent with post-traumatic stress disorder, anxiety, and/or depression evident by a total score of greater than or equal to 1.75 on Hopkins Symptoms Checklist-25 and/or by a total score greater than or equal to 2.5 on the Harvard Trauma Questionnaire Part 4
  • Presents with symptoms consistent with centralized pain evident by a score of greater than or equal to 40 on the Central Sensitization Inventory Part A.

Exclusion criteria

  • Reports he will not remain in the current reformatory for at least 6 months from the onset of the study
  • Is unable to make the time commitment required to participate
  • Presents with symptoms consistent with a psychiatric condition which makes participation in the study unsafe for himself or others, based on the evaluation by the treating psychotherapist
  • Presents with a high risk to self or others which makes participation in the study unsafe for himself or others, based on evaluation by the treating psychotherapist
  • Participation is deemed unsafe due to a severe medical condition previously diagnosed by a medical doctor and/or signs/symptoms consistent with a possible medical condition based on the evaluation by the treating physiotherapist, 6.) reports previously receiving treatment by Wchan
  • Current substance abuse reported by participant or identified by treating psychotherapist
  • Currently receiving mental health services and/or physiotherapy services from other organization
  • Reports unresolvable conflict with participant/s enrolled in the study.

Treatment and study plan

Physiotherapy

Other

Treatment group participants will participate in weekly group physiotherapy and psychotherapy sessions as part of the standard program procedure.

Psychotherapy

Other

Treatment group participants will participate in weekly group physiotherapy and psychotherapy sessions as part of the standard program procedure.

Primary outcomes

  1. Hopkins Symptom Checklist-25

    Time frame: 10 weeks

    The HSCL-25 is a 25-question symptom inventory which measures symptoms of anxiety and depression.

Secondary outcomes

  1. Patient Specific Functional Scale

    Time frame: 10-weeks

    This useful questionnaire can be used to quantify activity limitation and measure functional outcome for patients with any orthopaedic condition.

  2. Pittsburgh Sleep Quality Index

    Time frame: 10-weeks

    The Pittsburgh Sleep Quality Index (PSQI) is an effective instrument used to measure the quality and patterns of sleep in adults.

  3. Patient's Global Impression of Change Scale

    Time frame: 10-weeks

    The self-report measure Patient Global Impression of Change (PGIC) reflects a patient's belief about the efficacy of treatment

  4. General Self Efficacy Scale

    Time frame: 10-weeks

    The General Self-Efficacy Scale is a 10-item psychometric scale that is designed to assess optimistic self-beliefs to cope with a variety of difficult demands in life.

  5. Central Sensitization Inventory

    Time frame: 10-weeks

    This tool was published with the purpose of providing a single self-report instrument that identified symptoms associated with central sensitization and the quantified the degree of those symptoms.

  6. Harvard Trauma Questionnaire Part 4

    Time frame: 10 weeks

    The Harvard Trauma Questionnaire (HTQ) is a checklist that inquires about a variety of trauma events, as well as the emotional symptoms considered to be uniquely associated with trauma.

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Registry information

Official study title

A Randomized Controlled Wait-list Pilot Study Examining the Feasibility and Impact of a Combined Psychotherapy and Physiotherapy Group Treatment Program for Survivors of Torture Incarcerated in an Adult Prison in Kurdistan, Iraq

Important dates

Study start
2018
Primary completion
2018
Study completion
2019
First posted
Mar 20, 2018
Registry last updated
Mar 13, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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