The Effect of BAT Versus Mixed Physical Activity as add-on Treatment for Traumatised Refugees.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

338 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-09-30

Study Completion Date

2015-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this randomised controlled trial is to study two types of physical activities as add-on treatment, compared to treatment as usual for traumatised refugees. Hereby, the study will examine the evidence of an often-used treatment modality in a field where very little research yet has been conducted.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Traumatized Refugees -Stress Management Versus Cognitive Re-structuring

NCT01362543

Posttraumatic Stress Disorder

COMPLETED PHASE3

Cross-sectoral Collaboration in Multidisciplinary Treatment of Trauma-affected Refugees

NCT04244864

Post Traumatic Stress Disorder Depression Psychosocial Problem

COMPLETED NA

Treatment of Sleep Disturbances in Trauma-affected Refugees

NCT02761161

Post Traumatic Stress Disorder Depression

COMPLETED PHASE4

Arts and Movement Therapies for Trauma

NCT03515564

PTSD Depression Anxiety +2 more

COMPLETED NA

Early Prevention of PTSD in Patients Within One Week of Acute Physical Trauma

NCT02915497

Post Traumatic Stress Disorder

SUSPENDED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

About the clinic: The study will be carried out at the Competence Centre for Transcultural Psychiatry Denmark (CTP) (before January 2013 named Psychiatric Trauma Clinic for Refugees (PTF)). The clinic was established in 2008 and since 2009 the clinic has been carrying out randomised, controlled trials aiming to increase knowledge about the treatment effect of different types of treatment for traumatised refugees. The target group of the centre is traumatised refugees with PTSD, depression and anxiety. Patients are referred to CTP by general practitioners or psychiatrists. CTP treats approximately 200 patients/year.

The treatment is inter-disciplinary and consists of consultations with a medical doctor whereby pharmacological treatment according to best practice in the field is given, supplemented by cognitive behavioural therapy by a psychologist. Manuals are used for both the treatment given by the medical doctor as well as the psychologist. The total duration of treatment is 6 months.

Material and methods: 310 patients will be included from September 2013 to approximately May 2015. At the referral interview it is clarified whether the patient meets the inclusion or exclusion criteria. If the patient meets the inclusion criteria and gives her/his consent to participate, the patient is randomised to one of the three intervention groups:

A) Control group: receives treatment as usual (TAU) consisting of: 6 months of consultations and medical treatment according to best clinical practice by a medical doctor as well as manual-based Cognitive Behaviour Therapy by a psychologist.

B) Basic Body Awareness Therapy (BBAT): TAU + BBAT.

C) Mixed physical activity (MPA): TAU + MPA

The duration of B and C is 20 weeks each, 1 hour/week.

The physical activity will be on individual sessions.

* Quality assurance plan: Good Clinical Practice (GCP) is monitoring and auditing the project from the project's start to its end. Moreover, The Competence Centre for Transcultural Psychiatry (CTP) has a monitoring team monitoring the data being registered as data are coming in.
* Data checks: GCP as well as the before mentioned monitoring team will be doing data checks and auditing during the time the trial is running.
* Source data verification: to assess the accuracy, completeness and representativity of registry data, the monitoring team of CTP is during the trial comparing the data registered manually by doctors, psychologists, physiotherapist and social workers with e.g. the papers filled in by the patients themselves. Data registered from the patients in the trial are also registered from the patients that are not participating in the trial. By comparing those data, this will show the representativity of the data from this population.
* Standard Operating Procedures: All adverse events will be registered in the individual patient records in the period from the first consultation at the centre to the last consultation at the centre of each patient.

All Serious Adverse Events (SAEs) will be reported by sponsor or investigator to The National Committee on Health Research Ethics (within 7 days after investigator has become aware of any such), with comments enclosed on potential consequences for the trial.

Sponsor will yearly submit a report to The National Committee on Health Research Ethics on all SAEs, with an assessment attached on the security of the patients participating in the trial.

The report will be submitted each year on the day when the trial was given approval from The National Committee on Health Research Ethics.

A list of all patients screened for participating in the trial and of all patients finally included in the trial will be kept.

* Data dictionary: not relevant.
* Randomisation is carried out by the Department of Biostatistics at the University of Copenhagen, with practical assistance from a group of secretaries not linked to the daily work at CTP. The participants will be stratified by gender and severity of PTSD symptoms on the basis of Harvard Trauma Questionnaire (HTQ). Blinding of patients and practitioners is not considered to be possible, but intervention-group blinded Hamilton Depression and Anxiety ratings will be carried out at the beginning and at the end of treatment. The Hamilton raters are medical students trained at the clinic and take part in regular joint ratings to ensure high quality and inter-rater reliability.
* Data processing/statistical analysis:

Size of material and power calculation:

If 200 patients are divided into three groups of about 65 patients, power to detect a group difference in the treatment effect of ½ standard deviation (SD) will be 81%, while power to detect a difference of 1 SD will be close to 100%. Differences in quantitative outcomes less than ½ SD between the two treatments are considered to be less relevant from a clinical point of view. Cut-offs are available for several rating scales, and these can be used to define categorical outcome variables. If for example the proportions below cut-off for clinical case status are 50% and 25% in two groups, power will be close to 80% to detect a significant group differences.

Data analysis: The primary outcome variables are differences during the treatment course calculated as differences between start, middle and end ratings. The unadjusted differences between the two intervention groups can be measured by a t-test, while adjustment of the differences for baseline values and possible background factors (such as gender and age) can be done by ANCOVA/linear regression.

In addition, cut-off can be used on symptom scores and logistic regression analyses can be carried out with over/under cut-off as binary outcome. In addition to completer analyses, drop-out analysis and intention-to-treat analyses will be carried out.

Hypotheses concerning predictors of treatment effects can be analysed by including the potential predictors in linear or logistic regression models including treatment group and relevant covariates.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

PTSD Depression Pain

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control

Psychiatric treatment as usual for 6 months according to best clinical practice: 10 consultations with a medical doctor (medication and psycho-education) as well as 16 consultations with a psychologist.

Group Type ACTIVE_COMPARATOR

Control

Intervention Type OTHER

Psychiatric treatment as usual for 6 months according to best clinical practice.

Basic Body Awareness Therapy

Intervention Type OTHER

20 weeks, 1 hour/week.

Mixed physical activity

Intervention Type OTHER

20 weeks, 1 hour/week.

Basic Body Awareness Therapy

Standard psychiatric treatment + Basic Body Awareness Therapy for 20 weeks, 1 hour/week.

Group Type EXPERIMENTAL

Basic Body Awareness Therapy

Intervention Type OTHER

20 weeks, 1 hour/week.

Mixed physical activity

Standard psychiatric treatment + Mixed physical activity for 20 weeks, 1 hour/week.

Group Type EXPERIMENTAL

Mixed physical activity

Intervention Type OTHER

20 weeks, 1 hour/week.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Control

Psychiatric treatment as usual for 6 months according to best clinical practice.

Intervention Type OTHER

Basic Body Awareness Therapy

20 weeks, 1 hour/week.

Intervention Type OTHER

Mixed physical activity

20 weeks, 1 hour/week.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients referred to treatment for PTSD at Competence Centre for Transcultural Psychiatry from September 2013 to May 2015.
* Adults (18 years or older)
* Refugees or persons who have been brought in under family reunification
* Symptoms of PTSD pursuant to the International Classification of Diseases (ICD-10) research criteria.
* Psychological trauma in the anamnesis. Trauma is typically imprisonment or detention with torture (according to the United Nations definition of torture) or acts of cruel, inhuman and degrading treatment or punishment. Trauma can also be organised violence, long-term political persecution and harassment, or war and civil war experiences.
* Assessed by a doctor to be motivated for treatment
* Informed consent.

Exclusion Criteria

* Severe psychotic disorder (defined as patients with an ICD-10 diagnosis F2x and F30.1-F30.9). Patients are excluded only if the psychotic-like experiences are assessed to be part of an independent psychotic disorder and not part of a severe PTSD and/or depression.
* Current abuser of drugs and alcohol (F1x.24-F1x.26).
* In need of admission to psychiatric hospital.
* No informed consent.
* Physical handicaps that make the person unable to participate in the physical activity.
* Cardiac arrhythmia identified on the electrocardiogram taken before start of the treatment or symptoms of heart problems that are unclarified.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No