Modular Patient Centred CBT for Danish Veterans With Complex PTSD

Complex Post-Traumatic Stress Disorder Clinical Trial

— MPC  

Official title:

Modular Patient Centred CBT for Danish Veterans With Complex PTSD: A Randomised Controlled Pilot Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05259592
• Other study ID #: SJ-871
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: December 17, 2020
• Est. completion date: December 2026

Study information

• Verified date: February 2022
• Source: Danish Veterans Centre
• Contact: Sofie Folke, PhD
• Phone: 72163251
• Email: vetc-mpa43[@]mil.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Modular Patient Centred CBT (MPC) for Complex PTSD (CPTSD) is a manualized psychotherapy programme that consists of five treatment modules addressing 1) Affect dysregulation, 2) Disturbed relationships, 3) Negative self-concept, 4) PTSD symptoms and 5) Insomnia and trauma-related nightmares. This aim of this first pilot randomised controlled trial (RCT) is to increase chances of a future successful efficacy RCT (Phase III trial) comparing the efficacy (on symptoms of CPTSD and co-morbid disorders) of a flexible, patient-centred version of the MPC treatment programme (where the client actively participates in treatment decisions) with a control treatment, where the five treatment modules are delivered in a predefined order. The primary objective of the pilot study is to: 1. Assess the implementation of the trial process in terms of inclusion, implementation and data collection 2. Assess necessary resources, including the use of tablets for data collection, time spent on the project by participating therapists, assessing psychologists and secretaries The secondary objective is to: 1. Assess changes in symptoms of CPTSD between the intervention and control group as well as within each group 2. Examine changes in levels of comorbidity associated with CPTSD, such as anxiety, depression, insomnia, somatic complaints, drugs and alcohol intake between the intervention and control group as well as within each group 3. Examine changes in well-being, functioning and attachment style between the intervention and control group as well as within each group 4. Examine developments in client motivation and working alliance between the intervention and control group as well as within each group. 60 veterans with CPTSD are randomised to receive either the flexible, patient-centred version of the MPC treatment programme or the control treatment. The investigators will consider the study as complete if the following success criteria are met: 1. > 70% of potential participants accept and be included in the study 2. Completion rate of 70%, that is, the investigators expect to have complete end-of-treatment data of at least 70% of all participants included 3. Complete three-month follow-up of at least 50% of all participants included. The project neither collects new biological material nor biological material from existing biobanks. The project is based on questionnaire data.

Description:

ICD-11 complex PTSD (CPTSD) is a new diagnosis and up to this date, no effective treatment has been identified to help clients with this severe mental disorder. Therefore, it is very important that effective treatment methods for clients with CPTSD be identified. In 2019 the Danish Veteran Centre launched the development of a treatment programme for veterans with CPTSD; Modular Patient Centred CBT (MPC) for CPTSD. MPC is a manualised treatment programme that consists of 32 individual psychotherapy sessions, divided into an initial treatment module (two therapy sessions) and five treatment modules (each consisting of six therapy sessions) that can be combined in different ways to adapt to each client's most prominent symptoms, preferences and readiness (to work with exposure, for instance). The five treatment modules address 1) Affect dysregulation (6 sessions), 2) Disturbed relationships (6 sessions), 3) Negative self-concept (6 sessions), 4) PTSD symptoms (6 sessions) and 5) Insomnia and trauma-related nightmares (6 sessions). This first trial of the MPC treatment programme is conducted as a pilot randomised controlled trial. The primary objective of this study is to increase chances of a future successful efficacy RCT (Phase III trial) comparing the efficacy (on symptoms of CPTSD and co-morbid disorders) of a flexible, patient-centred version of the MPC treatment programme (where the client actively participates in treatment decisions) with a control treatment, where the five treatment modules are delivered in a predefined order; 1) Affect dysregulation, 2) Disturbed relationships, 3) Negative self-concept, 4) PTSD symptoms, and 5) Insomnia and trauma-related nightmares. The primary objective of the pilot study is to: 1. Assess the implementation of the trial process in terms of inclusion, implementation and data collection 2. Assess necessary resources, including the use of tablets for data collection, time spent on the project by participating therapists, assessing psychologists and secretaries The secondary objective is to: 1. Assess changes in symptoms of CPTSD, assessed with the International Trauma Questionnaire (ITQ; Cloitre et al., 2018) between the intervention and control group as well as within each group 2. Examine changes in levels of comorbidity associated with CPTSD, such as anxiety, depression, insomnia, somatic complaints, drugs and alcohol intake between the intervention and control group as well as within each group 3. Examine changes in well-being, functioning and attachment style between the intervention and control group as well as within each group 4. Examine developments in client motivation and working alliance between the intervention and control group as well as within each group. 60 veterans with CPTSD are randomised to receive either the flexible, patient-centred version of the MPC treatment programme or the control treatment. As an integral part of the treatment, a short assessment is conducted after each treatment module by having the client complete the primary outcome measure, the ITQ which is used as a measure for assessing ICD-11 PTSD and CPTSD. In practice, the client fills in the ITQ on a tablet in the beginning of the last session of each treatment module, after which the client and therapist receive an automatic response on the tablet, establishing whether the client (based on the ITQ) continues to meet the diagnostic criteria for PTSD or CPTSD. If the client has achieved sufficient symptom recovery and no longer meets the diagnostic criteria for CPTSD, the client is considered a treatment completer. However, the client and the therapist might decide to continue treatment until the client no longer meets the diagnostic criteria for PTSD. In this way, treatment can continue to up till 32 therapy sessions but client and therapist can end the treatment earlier if the client has a valid assessment and falls out of CPTSD criteria. Since the study is a pilot study, aiming to inform a future RCT, the investigators will consider the study as complete if the following success criteria are met: 1. > 70% of potential participants accept and be included in the study 2. Completion rate of 70%, that is, the investigators expect to have complete data (end-of-treatment outcome assessment completed at the final therapy session) of at least 70% of all participants included 3. Complete three-month follow-up of at least 50% of all participants included. The treatment is carried out at five local veteran centres in Denmark by clinical psychologists employed by the Military Psychology Department (MPD), Danish Veterans Centre. The participating psychologists receive training and regular method-specific supervision in the MPC treatment programme. The project neither collects new biological material nor biological material from existing biobanks. The project is based on questionnaire data

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 2026
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

• Meets the diagnostic criteria for CPTSD, assessed with the ITQ
• Danish veteran (cf. the Veteran Policy of Denmark )
• Seeks help at the Military Psychology Department, Danish Veterans Centre, for deployment-related psychological issues

Exclusion Criteria:

• Severely suicidal
• Current alcohol or drug abuse that prevents treatment
• Blast injuries or current severe attention disorder
• Has received psychotherapeutic treatment in the past three months
• Is participating in another research project that interferes with this study

Related Conditions & MeSH terms

• Complex Post-Traumatic Stress Disorder
• Stress Disorders, Post-Traumatic
• Stress Disorders, Traumatic

Intervention

Behavioral:
• Psychotherapy
Modular Patient Centred CBT (MPC) for CPTSD (Folke, Friis, Thomsen & Roitmann, 2020) is a psychotherapy treatment manual consisting of up to 32 individual therapy sessions broken down by five treatment modules (each consisting of six sessions) that directly address the symptoms of CPTSD: 1) Affect dysregulation, 2) Disturbed relationships, 3) Negative self-concept, 4) PTSD symptoms, and 5) Insomnia and trauma-related nightmares.

Locations

Country	Name	City	State
Denmark	Danish Veterans Centre, Aalborg Kaserner	Aalborg
Denmark	Danish Veterans Centre, Garderkasernen	Birkerød
Denmark	Danish Veterans Centre, Svanemoellen Kaserne	Copenhagen Ø
Denmark	Danish Veterans Centre, Ryes Kaserne	Fredericia
Denmark	Danish Veterans Centre; Ringsted Kaserne	Ringsted

Sponsors (3)

Lead Sponsor	Collaborator
Danish Veterans Centre	Edinburgh Napier University, University of Copenhagen

Country where clinical trial is conducted

Denmark, 

References & Publications (4)

Boutron I, Altman DG, Moher D, Schulz KF, Ravaud P; CONSORT NPT Group. CONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts. Ann Intern Med. 2017 Jul 4;167(1):40-47. doi: 10.7326/M17-0046. Epub 2017 Jun 20. — View Citation

Chan AW, Tetzlaff JM, Gøtzsche PC, Altman DG, Mann H, Berlin JA, Dickersin K, Hróbjartsson A, Schulz KF, Parulekar WR, Krleza-Jeric K, Laupacis A, Moher D. SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials. BMJ. 2013 Jan 8;346:e7586. doi: 10.1136/bmj.e7586. — View Citation

Cloitre M, Shevlin M, Brewin CR, Bisson JI, Roberts NP, Maercker A, Karatzias T, Hyland P. The International Trauma Questionnaire: development of a self-report measure of ICD-11 PTSD and complex PTSD. Acta Psychiatr Scand. 2018 Dec;138(6):536-546. doi: 10.1111/acps.12956. Epub 2018 Sep 3. — View Citation

Folke, S, Friis, K, Thomsen, U, & Roitmann, N. Modulopbygget Patient-centreret CBT til Kompleks-PTSD - behandlingsmanual version 1.0. Unpublished manual. 2020

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The International Trauma Questionnaire (ITQ; Cloitre et al., 2018)	20-item self-report scale that assesses the diagnostic criteria for PTSD and CPTSD according to ICD-11	Through study completion, up to 1 year
Secondary	The Insomnia Severity Index (ISI)	7-item self-report scale that assesses insomnia	Through study completion, up to 1 year
Secondary	The Depression Anxiety Stress Scales (DASS-42)	42-item self-reporting instrument designed to measure three related negative emotional stages of depression, anxiety and tension/stress	Through study completion, up to 1 year
Secondary	Item 1-12 from the Common Mental Disorders Questionnaire (CMDQ)	12 item self-report scale that assesses somatic symptoms	Through study completion, up to 1 year
Secondary	3 items from the Alcohol Use Disorders Identification Test (AUDIT).	Three questions about alcohol consumption; 1) how often the client consumes alcohol; 2) how many items the client consumes on a typical day, and 3) whether the client has been treated for alcohol abuse.	Through study completion, up to 1 year
Secondary	7 items on cannabis and other forms of drugs	Questions on cannabis and other forms of drugs. The questions have previously been used in surveys by the Danish Veteran Centre and the National Institute of Public Health, the University of Southern Denmark.	Through study completion, up to 1 year
Secondary	World Health Organization Well-being Index (WHO-5)	5 item self-report scale that assesses subjective psychological well-being	Through study completion, up to 1 year
Secondary	The Sheehan Disability Scale (SDS)	3 item self-report scale that assesses occupational, social and family functioning	Through study completion, up to 1 year
Secondary	The Experiences in Close Relationships - Short form (ECR-S)	12 item self-report scale that assesses adult attachment style	Through study completion, up to 1 year