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Cognitive Processing Therapy (CPT) Memory Support (MS) Study

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv11
  2. Minor Primary completion date: Dec 2026 to Jan 2027
    • Study completion date: Dec 2026 to Apr 2027
    v10
  3. Minor Re-verified, no change to tracked fieldsv9
  4. Minor Eligibility criteria expanded, about 1 wordv8
  5. Minor Re-verified, no change to tracked fieldsv7
Show 5 earlier versionsHide 5 earlier versions
  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jan 2023 to Jan 4, 2023
    • Site details revised
    v6
  2. Notable Start date: Nov 2022 to Jan 2023v5
  3. Notable Start date: Sep 2022 to Nov 2022
    • Study sites: 0 to 1
    • Collaborators: 1 to 2
    v4
  4. Notable Start date: Jul 2022 to Sep 2022v3
  5. Minor Re-verified, no change to tracked fieldsv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
889 trials monitored
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The efficacy of psychological interventions for posttraumatic stress disorder (PTSD) is likely limited by the difficulty participants have learning and remembering important therapy content. Accordingly, the present study will examine the utility of integrating a Memory Support (MS) intervention into Cognitive Processing Therapy (CPT), an empirically supported and widely disseminated treatment for PTSD. MS was designed to integrate techniques aimed at facilitating encoding, consolidation, and retrieval of new learning into existing treatments, and has been shown to improve outcomes when integrated into cognitive therapy for depression. A pilot randomized controlled trial (n=52) comparing CPT with Memory Support (CPT+MS) to CPT-alone will be conducted. Study participants will be adults diagnosed with PTSD. The primary aim of the trial will be to determine if CPT+MS will lead to greater memory and learning of therapy content relative to CPT-alone, and to establish the acceptability and feasibility of integrating MS into CPT. Secondary aims include a preliminary examination of treatment efficacy, as indicated by the magnitude of changes in PTSD symptoms between conditions, and target validation, as indicated by associations between memory and learning of therapy content and treatment response. Exploratory analyses will examine several indicators of baseline memory-related cognitive functioning as predictors of memory and learning of therapy content, providing preliminary data to inform future research on personalized application of MS. Results of the trial will advance scientific knowledge about methods for optimizing memory and learning as a mechanism for improving PTSD treatment outcomes.
Trial Details
NCT Number NCT05310097
Lead Sponsor Boston University
Collaborators: National Institute of Mental Health (NIMH), VA Boston Healthcare System
Conditions
(from sponsor)
PTSD
Related terms Stress Disorders, Post-Traumatic
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov