Improving PTSD Treatments for Adults With Childhood Trauma (IMPACT)
Primary Purpose
Post Traumatic Stress Disorder
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Trauma-focused treatment
Emotion regulation training
Intensive Trauma-focused treatment
Sponsored by
About this trial
This is an interventional treatment trial for Post Traumatic Stress Disorder
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of PTSD according to DSM-5, including at least one specific discrete memory of a traumatic event
- Multiple traumata related to childhood sexual/physical abuse that occurred before 18 years of age, and committed by a primary caretaker or an authority figure as index event
- Symptom severity: CAPS score > 25
- Sufficient fluency in Dutch to complete the treatment and research protocols
Exclusion Criteria:
- Involved in legal procedures concerning admission or stay in The Netherlands
- Involvement in compensation issues
- Pregnancy
- Severe non-suicidal self-injury (NSSI) in the last two months (hospital referral required)
- Suicidality in the last 2 months
- Alcohol or drug dependence in last 2 months
- Cognitive impairment (estimated IQ < 70)
- Changes in psychotropic medication in the two months prior to inclusion
- Current psychological treatment
Sites / Locations
- Leiden University - Institute of Psychology
- PsyQ department of psychotrauma
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Trauma-Focused Treatment
Emotion Regulation Treatment
Intensive Trauma-Focused Treatment
Arm Description
Weekly sessions of prolonged exposure
weekly sessions of emotion regulation and skills training.
prolonged exposure, 3 sessions per week
Outcomes
Primary Outcome Measures
PTSD symptom severity
Clinician Administered Posttraumatic Stress Inventory (CAPS-5) total score
Secondary Outcome Measures
Depressive symptom severity
total score on Inventory of Depressive Symptomatology (IDS)
Quality of Life score
EQ5D5L total score
Responder rate
Meeting pre-defined criteria for remission
Dropout rate
premature termination of treatment by patient
Emotion regulation
ICD-11 Trauma Questionnaire and Difficulties in Emotion Regulation Scale (DERS)
Self-reported PTSD symptoms
Post-traumatic Stress Disorder Checklist (PCL-5)
Interpersonal difficulties
ICD-11 Trauma Questionnaire and Inventory of Interpersonal Problems (IIP)
Self-concept
ICD-11 Trauma Questionnaire and Rosenberg self-esteem scale (RSS)
Full Information
NCT ID
NCT03194113
First Posted
June 19, 2017
Last Updated
February 16, 2021
Sponsor
Leiden University
Collaborators
Radboud University Medical Center, PsyQ, ZonMw: The Netherlands Organisation for Health Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT03194113
Brief Title
Improving PTSD Treatments for Adults With Childhood Trauma
Acronym
IMPACT
Official Title
Improving PTSD Treatments for Adults With Childhood Trauma
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
December 1, 2016 (Actual)
Primary Completion Date
April 15, 2019 (Actual)
Study Completion Date
December 19, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Leiden University
Collaborators
Radboud University Medical Center, PsyQ, ZonMw: The Netherlands Organisation for Health Research and Development
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this project is to investigate the effectiveness of phase-based trauma-focused therapy (PBT) and intensive trauma-focused therapy (I-TFT) for adult patients with PTSD related to childhood abuse.
We will carry out a RCT, randomizing 150 patients to receive either standard TFT, PBT or i-TFT. The effects will be assessed at two endpoints of treatment (4, 8 and 16 weeks) and after a 6 and 12 months follow-up in an intention-to-treat analysis.
Detailed Description
The Dutch treatment guidelines recommend trauma-focused treatment (TFT) for PTSD. In TFT, patients are exposed to trauma reminders that they typically avoid, until their emotional reactions decline. This treatment has been found very effective for some patients but there is much room for improvement, particularly in PTSD related to childhood abuse (CA-PTSD). Symptom exacerbation, non-attendance and dropout rates of up to 40% have been observed in patients with CA-PTSD.
Two alternative treatments have been proposed. Firstly, TFT may be preceded by emotion regulation and interpersonal skills training. This is called phase-based treatment (PBT). The rationale is that patients with CA-PTSD have affect regulation and interpersonal problems that interfere with effective delivery of TFT. These problems are rooted in the detrimental developmental effects of abuse (often by an attachment figure). PBT indeed resulted in more favorable outcomes and fewer dropouts. In international guidelines, PBT was recently recommended as treatment of choice for patients with CA-PTSD and comorbidity.
Another innovative treatment is intensive TFT (i-TFT), which means delivering TFT in 4 instead of 16 weeks. The condensed format enhances learning and prevents the buildup of anticipatory anxiety, which in turn affects the patients' motivation. Patients with CA-PTSD are also characterized by high psychosocial stressors, leading to problems with treatment attendance and compliance. The condensed format may improve motivation, attendance and compliance. I-TFT was recently tested in a case series in patients with CA-PTSD and in a randomized controlled trial (RCT) with patients with adulthood-related PTSD. Both studies had very low dropout rates (0-3%) and fast recovery.
The aim of the current study is to investigate the (cost)effectiveness of two innovative forms of trauma-focused therapy for patients with CA-PTSD: phase-based therapy (emotion regulation skills training followed bij PE) and intensive PE (i-PE). The effects will be assessed post-treatment and after a 6 and 12 months follow-up in an intention-to-treat analysis. Results will be disseminated and included in treatment guidelines. The ultimate goal is to improve quality of care and contribute to treatment innovation for this severely ill target population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Traumatic Stress Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Trauma-Focused Treatment
Arm Type
Active Comparator
Arm Description
Weekly sessions of prolonged exposure
Arm Title
Emotion Regulation Treatment
Arm Type
Active Comparator
Arm Description
weekly sessions of emotion regulation and skills training.
Arm Title
Intensive Trauma-Focused Treatment
Arm Type
Active Comparator
Arm Description
prolonged exposure, 3 sessions per week
Intervention Type
Behavioral
Intervention Name(s)
Trauma-focused treatment
Other Intervention Name(s)
Cognitive Behavior therapy, Prolonged exposure, Imaginal exposure
Intervention Description
Weekly sessions
Intervention Type
Behavioral
Intervention Name(s)
Emotion regulation training
Intervention Description
Managing and tolerating negative emotions, e.g. anger, sadness. Weekly sessions; preparatory to Prolonged exposure treatment
Intervention Type
Behavioral
Intervention Name(s)
Intensive Trauma-focused treatment
Other Intervention Name(s)
Intensive Prolonged Exposure
Intervention Description
Intensive version (3 sessions per week) of Trauma-focused treatment
Primary Outcome Measure Information:
Title
PTSD symptom severity
Description
Clinician Administered Posttraumatic Stress Inventory (CAPS-5) total score
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Depressive symptom severity
Description
total score on Inventory of Depressive Symptomatology (IDS)
Time Frame
16 weeks
Title
Quality of Life score
Description
EQ5D5L total score
Time Frame
16 weeks
Title
Responder rate
Description
Meeting pre-defined criteria for remission
Time Frame
16 weeks
Title
Dropout rate
Description
premature termination of treatment by patient
Time Frame
16 weeks
Title
Emotion regulation
Description
ICD-11 Trauma Questionnaire and Difficulties in Emotion Regulation Scale (DERS)
Time Frame
16 weeks
Title
Self-reported PTSD symptoms
Description
Post-traumatic Stress Disorder Checklist (PCL-5)
Time Frame
16 weeks
Title
Interpersonal difficulties
Description
ICD-11 Trauma Questionnaire and Inventory of Interpersonal Problems (IIP)
Time Frame
16 weeks
Title
Self-concept
Description
ICD-11 Trauma Questionnaire and Rosenberg self-esteem scale (RSS)
Time Frame
16 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of PTSD according to DSM-5, including at least one specific discrete memory of a traumatic event
Multiple traumata related to childhood sexual/physical abuse that occurred before 18 years of age, and committed by a primary caretaker or an authority figure as index event
Symptom severity: CAPS score > 25
Sufficient fluency in Dutch to complete the treatment and research protocols
Exclusion Criteria:
Involved in legal procedures concerning admission or stay in The Netherlands
Involvement in compensation issues
Pregnancy
Severe non-suicidal self-injury (NSSI) in the last two months (hospital referral required)
Suicidality in the last 2 months
Alcohol or drug dependence in last 2 months
Cognitive impairment (estimated IQ < 70)
Changes in psychotropic medication in the two months prior to inclusion
Current psychological treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Willem Van Der Does, PdhD
Organizational Affiliation
head of department of clinical psychology
Official's Role
Study Chair
Facility Information:
Facility Name
Leiden University - Institute of Psychology
City
Leiden
State/Province
Zuid-Holland
ZIP/Postal Code
2333 AK
Country
Netherlands
Facility Name
PsyQ department of psychotrauma
City
The Hague
State/Province
Zuid-Holland
ZIP/Postal Code
2333 AK
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported from this study may be shared, after deidentification
IPD Sharing Time Frame
Beginning 6 months and ending 5 years following article publication.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal.
Citations:
PubMed Identifier
16382429
Citation
Zayfert C, Deviva JC, Becker CB, Pike JL, Gillock KL, Hayes SA. Exposure utilization and completion of cognitive behavioral therapy for PTSD in a "real world" clinical practice. J Trauma Stress. 2005 Dec;18(6):637-45. doi: 10.1002/jts.20072.
Results Reference
background
Citation
Hendriks, L., & Van Minnen, A. (2014). What to do with treatment failures: Intensive (Prolonged) Exposure treatment for PTSD. Presentation at EABCT Conference The Hague.
Results Reference
background
PubMed Identifier
24480899
Citation
Ehlers A, Hackmann A, Grey N, Wild J, Liness S, Albert I, Deale A, Stott R, Clark DM. A randomized controlled trial of 7-day intensive and standard weekly cognitive therapy for PTSD and emotion-focused supportive therapy. Am J Psychiatry. 2014 Mar;171(3):294-304. doi: 10.1176/appi.ajp.2013.13040552.
Results Reference
background
PubMed Identifier
20595411
Citation
Cloitre M, Stovall-McClough KC, Nooner K, Zorbas P, Cherry S, Jackson CL, Gan W, Petkova E. Treatment for PTSD related to childhood abuse: a randomized controlled trial. Am J Psychiatry. 2010 Aug;167(8):915-24. doi: 10.1176/appi.ajp.2010.09081247. Epub 2010 Jul 1.
Results Reference
background
Citation
Cloitre, M., Courtois, C.A., Ford, J.D., Green, B.L., Alexander, P., Briere, J. et al. (2012). The ISTSS Expert Consensus Treatment Guidelines for Complex PTSD in Adults. http://www.istss.org/AM/Template.cmf?Section=ISTSS_Complex_PTSD_Treatment_Guidelines&Template=/CM/ContentDisplay.cfm&ContentID=5185
Results Reference
background
PubMed Identifier
34630934
Citation
Oprel DAC, Hoeboer CM, Schoorl M, de Kleine RA, Cloitre M, Wigard IG, van Minnen A, van der Does W. Effect of Prolonged Exposure, intensified Prolonged Exposure and STAIR+Prolonged Exposure in patients with PTSD related to childhood abuse: a randomized controlled trial. Eur J Psychotraumatol. 2021 Jan 15;12(1):1851511. doi: 10.1080/20008198.2020.1851511. eCollection 2021.
Results Reference
derived
PubMed Identifier
30541492
Citation
Oprel DAC, Hoeboer CM, Schoorl M, De Kleine RA, Wigard IG, Cloitre M, Van Minnen A, Van der Does W. Improving treatment for patients with childhood abuse related posttraumatic stress disorder (IMPACT study): protocol for a multicenter randomized trial comparing prolonged exposure with intensified prolonged exposure and phase-based treatment. BMC Psychiatry. 2018 Dec 12;18(1):385. doi: 10.1186/s12888-018-1967-5.
Results Reference
derived
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Improving PTSD Treatments for Adults With Childhood Trauma
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