Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05407337
Other study ID # 2021-A01172-39
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 22, 2022
Est. completion date February 15, 2025

Study information

Verified date July 2023
Source Assistance Publique Hopitaux De Marseille
Contact Clotilde IZABELLE, Dr
Phone 0660536125
Email clotilde.izabelle@ap-hm.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Displaced people, like refugees or asylum seekers, have high rate of potentially traumatic events. PTSD is one of the most common psychiatric trouble in this population. It requires specialized support and psychosocial program. Narrative Exposure Therapy (NET), a german psychotherapy, was developed in the 2000 to specifically treat psycho-trauma in this population. It is brief, effective on complex trauma and can be delivered by trained non-caregivers. All published randomized studies have conclued that NET is effetive, but there are still insifficient numbers to make recomendations. To our knowledge, NET has never been tested in France. In Marseille, SINDIANE is a community support and program for refugees and asylum seekers. Many workshops led by peer workers are offered to increase empowerment of beneficiaries and hel them to recover. The development of a NET workshop would make it possible to combine community support and specific and validated psychotherapy. Through this study, the investigators hypothesize that tratment of PTSD with NET in the community-based SINDIANE program decrease symptoms of PTSD.


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).


Recruitment information / eligibility

Status Recruiting
Enrollment 46
Est. completion date February 15, 2025
Est. primary completion date August 15, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Psychotherapy using Narrative Exposure Therapy (NET)
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.

Locations

Country Name City State
France Assistance Publique Hôpitaux Marseille Marseille Bouches-du-Rhône

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary PTSD symptoms measure by PCL5 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
= A little bit
= Moderately
= Quite a bit
= Extremely
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
Secondary Evolution of PCL5 score 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
= A little bit
= Moderately
= Quite a bit
= Extremely
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
Secondary Psychiatric comorbidity intensity score RHS15 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
= A little bit
= Moderately
= Quite a bit
= Extremely A score of 0 means that the patient does not have a psychiatric disorder. The higher the score, the more the patient will have more and more mental disorders.
before the intervention, 1 month post therapy, 3 months and 6 months
Secondary EvExperience indicators intensity score (GSE) 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
See also
  Status Clinical Trial Phase
Terminated NCT05189977 - A Trial to Assess the Effects of Prazosin or Propranolol on Blood Pressure in the Presence of Brexpiprazole/Sertraline Phase 1
Completed NCT01806168 - rTMS in the Treatment of PTSD N/A
Not yet recruiting NCT06194851 - Examining Intranasal Oxytocin Augmentation of Brief Couples Therapy for Veterans With PTSD Phase 2
Completed NCT02187224 - Progesterone Effect on Individuals Diagnoses With AD and PTSD. Phase 2/Phase 3
Completed NCT02549508 - Comparison Study Using APAP With and Without SensAwake in Patients With OSA and PTSD N/A
Not yet recruiting NCT01940549 - Transcranial Direct Current Stimulation (tDCS) Enhancement of Trauma-focused Therapy for Posttraumatic Stress Disorder N/A
Completed NCT02012738 - Treatment of Trauma and Violence in the Townships of South Africa N/A
Terminated NCT03209882 - Transcranial Infrared Laser Stimulation (TILS) of Prefrontal Cognition in Post-traumatic Stress Disorder (PTSD) N/A
Completed NCT04891614 - The PRISM Pilot Trial for Post-Traumatic Stress Disorder N/A
Completed NCT02030522 - Prospective Cohort Study of Accelerated Resolution Therapy (ART) for Treatment of Military Psychological Trauma N/A
Completed NCT01729325 - Prevention of Post-Traumatic Stress Disorder in Soldiers Phase 2
Completed NCT02053532 - Functional Brain Imaging in PTSD N/A
Not yet recruiting NCT02598024 - Treating Earthquake in Nepal Trauma (TENT) Trial 2016 N/A
Terminated NCT02237703 - Kappa Opioid Receptor Imaging in Post-traumatic Stress Disorder (PTSD) N/A
Withdrawn NCT02356861 - LED Light Therapy to Improve Cognitive & Psychosocial Function in TBI-PTSD Veterans N/A
Not yet recruiting NCT05974631 - Evaluating Treatments for Suicidal Veterans With PTSD N/A
Not yet recruiting NCT06288594 - TraumaRelief App: A Pilot RCT Assessing Feasibility and Acceptability N/A
Completed NCT01847469 - Zonisamide in Addition to E-CPT-C for Veterans With PTSD and Comorbid Alcohol Dependence Phase 2
Terminated NCT02237677 - CB1 Receptor PET Imaging Reveals Gender Differences in PTSD N/A
Completed NCT01691092 - PET Imaging of mGLuR5 With Drug Challenge N/A