- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05407337
The Effect of Narrative Exposure Therapy Intervention on Post-traumatic Stress Dissorder and Personal Recovery in Refugees and Asylum Seekers of Sindiane Programme (SINDIANE)
Single Center, Randomized, Comparative, Prospective Interventional Study Evaluating the Impact of Brief Psychotherapy by Narrative Exposure Therapy (NET) on the Reduction of Symptoms of Post Traumatic Stress Disorder in Refugee and Asylum Seeking Women in the Program SINDIANE in Marseille
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Methods and design Forty-six participants with a diagnosis of PTSD disorder within the SINDIANE program will be recruited. A prospective single-blind randomized clinical trial will be conducted comparing two groups, one participant in the classic SINDIANE program and one being treated in addition by NET workshp. The evaluations will be done at the baseline, after the intervention and at three and six months follow-up. IN addition, the qualitative and participatory research method called photovoice will be used to better understand the experiences of participants who recieve NETtroughout their recovery.
The primary objective is the assessment of the symptom intensity score (PCL-5) of posttraumatic stress disorder (PTSD).
Secondary objectives are represented by:
- The assessment of the stability over time of the PTSD symptom intensity score at three months and six months (PCL-5).
- Assessment of the intensity of global psychiatric comorbidities (RHS-15)
- Evaluation of life indicators: ability to act, quality of life (GSE self-efficacy questionnaire).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Bouches-du-Rhône
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Marseille, Bouches-du-Rhône, France, 13354
- Assistance Publique Hôpitaux Marseille
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Woman over 18
- Refugee or asylum seeker (habing applied to OFFPRA or with a residence permit)
- Belonging to the SINDIANE community project
- Having been exposed to at least one traumatic event (according to the DSM 5 definition validated by a doctor)
- Having a PCL5 score greater than 23
- Agreeing to participate in the study with an informed consent signed by the subject after explanations given by the investigating psychiatrist
- Patient affiliated to a social security health care
- Patient able to read and write arabic or french
Exclusion Criteria:
- Be under the age of 18
- Be included in another intervention research
- Presence of severe mental retardation or dementia according to DSM5
- Persons benefiting from special protection : under article L3212-1 and L3213-1 of the Public Health Code
- Persons referred to in articles L1121-5 to L1121-8 of the CSP
- Existence of a high suicide risk assessed by the R.U.D.
- Patient subject to a compulsory care measure (Law n°2011-803 of july 5, 2011 relating to the rights and protection of persons subject to psychiatric care and the terms of care)
- Patient refusing to sign the consent or unable to receive the information necessary to give informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Beneficiaries of NET therapy + standard Sindiane program management.
|
There are four NET sessions, each lasting thirty minutes and defined in advance on a weekly basis. The first session is the one where the person concerned will establish his/her "Life Line" and start his/her life story with the peer mediator. The second and third session will be the one where the person will continue his life story. Each session will begin with the mediator reading the story from the previous session, with the person concerned modifying the story if they wish. The fourth session will also start with the reading of the story from the previous session and will finish the story if necessary. It will also be the occasion to give the printed story to the person concerned at the end of the session and have it signed by the mediator and the patient. To prevent a possible risk of decompensation of the subject during the session, there will be a psychiatrist on site at the time of the NET to be available if the patient needs it. |
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No Intervention: Control group
Beneficiaries of the standard care of the Sindiane program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PTSD symptoms measure by PCL5
Time Frame: 1 month post NET therapy
|
The PCL-5 is a self reported score. The higher the score, the greater intensity of the symptoms of PTSD. It is validated in english and french with goof psychometric characteristic. The total score of the questionnaire is 80. The scale varies per question from 0 to 4: 0 = Not at all
If the patient gets a 0, it means that he/she does not have this symptom of post-traumatic stress. On the contrary, the more the score increases and tends towards 4, the more the symptom will be present in the patient. |
1 month post NET therapy
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of PCL5 score
Time Frame: 3 months and 6 months
|
Comparaison of the PCL-5 score after therapy and at 3 and 6 moth. This endpoint is intersted in highlighting a possible improvement in symptoms at a distance from the therapy. The total score of the questionnaire is 80. The scale varies per question from 0 to 4: 0 = Not at all
If the patient gets a 0, it means that he/she does not have this symptom of post-traumatic stress. On the contrary, the more the score increases and tends towards 4, the more the symptom will be present in the patient. |
3 months and 6 months
|
|
Psychiatric comorbidity intensity score RHS15
Time Frame: before the intervention, 1 month post therapy, 3 months and 6 months
|
Since post traumatic stress disorder is often accompanied by comorbid disorders such as depression or addictive behavior disorder. This evaluation will allow us to assess the possible effectiveness of NET on the associated disorder. This judgment criterion will be assessed using RHS15 wich is a self administrated questionnaire validated in the creening of the main psychiatric disorders. The total of the base varies between 0 and 56. By question the scale varies between 0 and 4: 0 = Not at all
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before the intervention, 1 month post therapy, 3 months and 6 months
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EvExperience indicators intensity score (GSE)
Time Frame: before the intervention, 1 month post therapy, 3 months and 6 months
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This main judgment criterion is concerned with the overall functioning of person concerned. Indeed, it makes it possible to evaluate the satisfaction and the power to act of the person. It is used to have a broader assesment of the expected benefits of PTSD treatment. The total score varies between 10 and 40. The more the patient scores, the higher his or her sense of self-efficacy. |
before the intervention, 1 month post therapy, 3 months and 6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Clotilde IZABELLE, Dr, Assistance Publique Hôpitaux Marseille
- Study Director: François CREMIEUX, Assistance Publique Hôpitaux Marseille
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-A01172-39
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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