NCT06680193

Brief Summary

The current study will examine daily-level impacts of a technique addressing positive memory retrieval on thoughts, feelings, and health among individuals with trauma experiences.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

March 11, 2022

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 5, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

October 30, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

November 8, 2024

Completed
Last Updated

November 8, 2024

Status Verified

October 1, 2024

Enrollment Period

2.2 years

First QC Date

October 30, 2024

Last Update Submit

November 6, 2024

Conditions

Keywords

Posttrauma HealthPositive Autobiographical MemoriesTrauma

Outcome Measures

Primary Outcomes (6)

  • Daily negative and positive affect levels

    Daily Positive and Negative Affect are assessed by rating the extent of four positive (excited, cheerful, satisfied, relaxed) and six negative (stressed, irritated, anxious, sad, hopeless, insecure) emotions. This is adapted from the 20-item Positive and Negative Affect Scale. The total positive affect subscale score can range from 1 to 20, with higher scores reflecting more positive affect levels. The total negative affect subscale score can range from 1 to 30, with higher scores reflecting more negative affect.

    Each day for 21 days prior to and after the intervention and each survey references the past 24 hours

  • Daily positive events

    Daily positive events is measured by 1 item which asked participants to think about the most positive event of the day and rate how pleasant it was. The score can range from 1 to 4, with higher scores reflecting that the event was more pleasant.

    Each day for 21 days prior to and after the intervention and each survey references the past 24 hours

  • Daily posttrauma cognitions

    A 9-item brief version of the Posttraumatic Cognitions Inventory (PTCI-9) will measure trauma-related thoughts/beliefs with the time frame modified to 'in the last 24 hours.' The total raw score can range from 1 to 63, with higher scores reflecting endorsement of more negative posttrauma cognitions.

    Each day for 21 days prior to and after the intervention and each survey references the past 24 hours

  • Daily PTSD symptoms

    Daily-life version of the Primary Care-PTSD-5 screen (PC-PTSD-5) will assess daily PTSD symptoms with the time frame modified to 'in the last 24 hours.' The total score can range from 0 to 5, with higher scores reflecting endorsement of more PTSD symptoms.

    Each day for 21 days prior to and after the intervention and each survey references the past 24 hours

  • Number of retrieved positive memories

    AMT assesses the number of retrieved positive memories by using five cue words followed by a prompt to recall a personally meaningful and specific memory of an event that took place within any 24-hour period. The total score could range from 0 to 5, with higher scores indicating more number of retrieved positive memories.

    Baseline survey approximately 4 weeks prior to the intervention

  • Number of retrieved positive memories

    AMT assesses the number of retrieved positive memories by using five cue words followed by a prompt to recall a personally meaningful and specific memory of an event that took place within any 24-hour period. The total score could range from 0 to 5, with higher scores indicating more number of retrieved positive memories.

    1 week after intervention sessions

Secondary Outcomes (6)

  • Positive Emotion Dysregulation

    Baseline survey approximately 4 weeks prior to the intervention

  • Positive Emotion Dysregulation

    1 week after intervention sessions

  • Positive Emotion Dysregulation

    At each of the 4 weekly intervention sessions and each survey references the past week

  • PTSD symptom severity

    Baseline survey approximately 4 weeks prior to the intervention

  • PTSD symptom severity

    1 week after intervention sessions

  • +1 more secondary outcomes

Study Arms (1)

Processing of Positive Memories Technique

EXPERIMENTAL

PPMT was administered as a 4-session protocol in this arm.

Behavioral: Processing of Positive Memories Technique

Interventions

PPMT was administered weekly as a 4-session protocol. In session 1, participants receive psychoeducation on PTSD symptoms, an overview of PPMT, and are assessed for psychological symptoms. Sessions 1-4 involve the detailed processing of a salient positive autobiographical memory to elicit "values, affect, strengths, and thoughts" related to that positive memory. Homework assignments include listening to an audio recording of that memory, completing a "values, affect, strengths, and thoughts" log, and engaging in a behavioral activity. In session 4, the therapist also reviews psychological symptoms and addresses termination.

Processing of Positive Memories Technique

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • being aged between 18 and 65 years
  • endorsing a trauma with posttrauma symptoms
  • access to an electronic device with internet capabilities
  • working knowledge of English
  • being a current resident of the Dallas Fort Worth metroplex
  • willingness and availability to participate in approximately 10 weeks of this study (including 4 therapy sessions)
  • willingness to be video-recorded during sessions for quality control purposes

You may not qualify if:

  • active suicidal plan, suicidal attempt, homicidal plan, or homicidal attempt (past 3 months including current)
  • currently in therapy with a mental health provider

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of North Texas

Denton, Texas, 76201, United States

Location

Related Publications (2)

  • Greene T, Contractor AA, Dicker-Oren SD, Fentem A, Sznitman SR. The Effects of the Processing of Positive Memories Technique on Posttrauma Affect and Cognitions Among Survivors of Trauma: Protocol for a Daily Diary Study. JMIR Res Protoc. 2024 Jan 12;13:e51838. doi: 10.2196/51838.

    PMID: 38214953BACKGROUND
  • Rodenbaugh MM, Thompson LM, Sznitman SR, Jin L, Contractor AA. Refining processing of positive memories technique: client perspectives on components, format, and feasibility. Eur J Psychotraumatol. 2025 Dec;16(1):2563197. doi: 10.1080/20008066.2025.2563197. Epub 2025 Oct 9.

MeSH Terms

Conditions

Stress Disorders, Post-TraumaticWounds and Injuries

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 30, 2024

First Posted

November 8, 2024

Study Start

March 11, 2022

Primary Completion

June 5, 2024

Study Completion

June 5, 2024

Last Updated

November 8, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will share

All de-identified IPD will be shared.

Shared Documents
STUDY PROTOCOL, ICF
Time Frame
De-identified IPD will be shared in 2029 until 2034.
Access Criteria
De-identified IPD will be stored with limited access in a data repository. Any interested researchers will email the PIs and complete a data sharing contract. If the contract is approved by the PIs, data will be shared in a secure manner.

Locations