The Course and Outcome of Integreated Trauma and Addiction Treatment Between PTSD and CPTSD
NCT ID: NCT06588309
Last Updated: 2024-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
50 participants
OBSERVATIONAL
2023-09-01
2025-12-31
Brief Summary
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Detailed Description
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Objective: To determine differences in course and outcome of integrated trauma-focused treatment delivered alongside addiction treatment in participants with comorbid PTSD and CPTSD.
Study design: An observational, prospective study with two groups (N = 50, allocation ratio 1:1) of participants with a SUD. One group has a comorbid PTSD (n = 25) and the other a comorbid CPTSD (n = 25). Assessments take place at baseline (T0), after every trauma- focused treatment session (T11-9) and after 10 weeks during which trauma-focused treatment may or may not have been completed or prematurely terminated (T2).
Study population: Patients with SUD and either comorbid PTSD or CPTSD, aged ≥ 18 years, with good Dutch language proficiency, who receive addiction treatment and trauma-focused treatment and who provide written informed consent.
Intervention: Treatment as usual (TAU), in accordance with the Dutch clinical practice guidelines consists of 1) addiction treatment according to the Community Reinforcement Approach (henceforth CRA) and 2) trauma-focused treatment (EMDR-therapy, henceforth EMDR).
Main study parameters/endpoints: Changes in PTSD symptom severity in participants with comorbid PTSD and CPTSD from T0 to T2, as measured by the PCL-5 and CAPS-5.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: All participants receive TAU, both CRA and EMDR, including standardized assessments. Additionally, participants fill in one extra questionnaire (ITQ) at T0 and T2 and the CAPS is administered additionally at T2. The extra burden of filling the ITQ is approximately one minute and for the CAPS approximately ten to forty-five minutes depending on the amount of symptoms after trauma treatment. Given the observational nature of the study, no risks related to the study are expected beyond those associated with routine clinical addiction care (e.g. relapse).
To optimize data-collection, especially after termination of EMDR before T2 assessment, participants receive an incentive, a voucher worth 10 euro, after completing the baseline (T0) assessment and the first five PCL-5 assessments (T11-5), and a voucher worth 15 euro after completing the next four PCL-5 assessments (T16-9) and the final assessment (T2).
Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Addiction and PTSD
Eye movement desensitization and reprocessing (EMDR)
Integrated addiction and traumafocused treatment.
CRA
CRA is a comprehensive cognitive behavioural treatment that focuses on helping people discover and adopt a pleasurable, social and healthy lifestyle that is more rewarding than a lifestyle including substance use.
Addiction and CPTSD
Eye movement desensitization and reprocessing (EMDR)
Integrated addiction and traumafocused treatment.
CRA
CRA is a comprehensive cognitive behavioural treatment that focuses on helping people discover and adopt a pleasurable, social and healthy lifestyle that is more rewarding than a lifestyle including substance use.
Interventions
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Eye movement desensitization and reprocessing (EMDR)
Integrated addiction and traumafocused treatment.
CRA
CRA is a comprehensive cognitive behavioural treatment that focuses on helping people discover and adopt a pleasurable, social and healthy lifestyle that is more rewarding than a lifestyle including substance use.
Eligibility Criteria
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Inclusion Criteria
* A DSM-5 diagnosis of PTSD (n=25). A DSM-5 diagnosis of PTSD and an additional ICD-11 diagnosis of CPTSD (n=25).
* Planned start of EMDR-therapy within 8 weeks.
* Good Dutch language proficiency (based on clinical judgement).
* Written informed consent
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Radboud University Medical Center
OTHER
IrisZorg
OTHER
Responsible Party
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Locations
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IrisZorg
Arnhem, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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Wiebren Markus, PhD
Role: backup
Other Identifiers
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CPTSS
Identifier Type: -
Identifier Source: org_study_id
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