Examining Effects of a Therapeutic Focus on Positive Memories on Post-Trauma Health
Examination and Refinement of a Novel Treatment for Posttraumatic Stress Disorder: Processing of Positive Memories Technique (PPMT)
1 other identifier
interventional
70
1 country
1
Brief Summary
Posttraumatic stress disorder (PTSD) has devastating health consequences. Evidence-based PTSD interventions address the substantial burden of PTSD on the health of individuals and societies; however, several individuals receiving these interventions drop out and not all individuals experience improvement in PTSD symptoms. Moreover, these current PTSD interventions primarily target trauma memories. Notably, growing evidence suggests that PTSD symptoms are related to difficulties in the encoding and retrieving of positive memories as well. Thus, the proposed study will examine effects of and targets underlying a novel PTSD technique focused on narrating and detailing positive memories - Processing of Positive Memories Technique (PPMT). Methodologically, 70 individuals will be randomly assigned to PPMT vs. Supportive Counseling (SC) for this study. The aims of the proposed study include (1) examining PPMT's effects on PTSD symptom severity and stress systems' dysregulation (i.e., awakening salivary alpha amylase \[sAA\] and cortisol); (2) examining mechanisms underlying PPMT's effects; and (3) refining PPMT. It is hypothesized that the PPMT arm will report greater decreases in PTSD severity and sAA/cortisol ratios. Further, it is hypothesized that PPMT-related improved affect will mediate the association between study arm (PPMT vs. SC) and changes in PTSD severity. Lastly, feedback will be obtained from study participants on PPMT's feasibility, format, and content to refine PPMT. The proposed study may contribute preliminary evidence on the potential significance of targeting positive memories in PTSD interventions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 24, 2022
CompletedFirst Posted
Study publicly available on registry
August 31, 2022
CompletedStudy Start
First participant enrolled
February 23, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 19, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 19, 2025
CompletedSeptember 29, 2025
September 1, 2025
2 years
August 24, 2022
September 23, 2025
Conditions
Outcome Measures
Primary Outcomes (8)
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Baseline
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Week 1 post-baseline during therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Week 2 post-baseline during therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Week 3 post-baseline during therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Week 4 post-baseline during therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
Week 5 post-baseline during therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
1 week after last therapy session
Posttraumatic Stress Disorder Checklist for DSM-5 scores
PTSD symptom severity is assessed using 20 items with response options ranging from 0 = not at all to 4 = extremely.
3-month post treatment completion
Secondary Outcomes (9)
Saliva Samples
3 times each day for 2 consecutive days prior to first therapy session
Saliva Samples
3 times each day for 2 consecutive days after the last therapy session
Positive and Negative Affect Schedule
Baseline
Positive and Negative Affect Schedule
Week 1 post-baseline during therapy session
Positive and Negative Affect Schedule
Week 2 post-baseline during therapy session
- +4 more secondary outcomes
Study Arms (2)
Processing of Positive Memories Technique (PPMT)
ACTIVE COMPARATORParticipants receive 5 60-minute Processing of Positive Memories Technique (PPMT) sessions for PTSD following the treatment procedures as outlined in PPMT therapy manual.
Supportive Counseling (SC)
ACTIVE COMPARATORParticipants receive 5 60-minute supportive counseling (SC) sessions. SC includes a discussion of the daily monitoring diary and exploration of current issues and concerns.
Interventions
PPMT comprises of 5 sessions focused on identifying and processing positive memories. In Session 1-5, participants narrate details of one positive memory, and process the positive memory to elicit positive values, affect, strengths, and thoughts.
SC is a 5-session, active and non-specific treatment administered weekly, which includes a discussion of the daily monitoring diary and exploration of current issues and concerns.
Eligibility Criteria
You may qualify if:
- years old
- Willing/able to provide informed consent
- Past month DSM-5 posttraumatic stress disorder (PTSD) diagnosis
- Working knowledge of English
You may not qualify if:
- Active suicidal intent or attempts
- Active psychosis
- Currently receiving mental health therapy (past 3 months)
- Dosage changes in psychiatric medications (past 3 months)
- Currently pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of North Texas
Denton, Texas, 76203, United States
Related Publications (1)
Contractor AA, Blumenthal H, Rosenfield D, Shea MT, Taylor DJ, Fentem A, Vingren JL. Study protocol and rationale for a pilot randomized clinical trial comparing processing of positive memories technique with supportive counseling for PTSD. Contemp Clin Trials. 2024 Mar;138:107455. doi: 10.1016/j.cct.2024.107455. Epub 2024 Jan 20.
PMID: 38253251DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ateka Contractor, PHD
University of North Texas Health Science Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
August 24, 2022
First Posted
August 31, 2022
Study Start
February 23, 2023
Primary Completion
February 19, 2025
Study Completion
February 19, 2025
Last Updated
September 29, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share