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NCT06956781 · ClinicalTrials.gov registry record · NA

Multiphase Optimization Strategy (MOST) for Treating Pediatric Post-traumatic Stress Disorder (PTSD)

A NA study of PTSD and Trauma, sponsored by University of Rochester.

Recruiting
Registry status
NA
Development phase
200
Enrollment target
1
Study location

NCT06956781: Recruiting NA study of PTSD and Trauma, sponsored by University of Rochester.

NCT06956781 is a NA study of PTSD and Trauma that is actively recruiting participants, run by University of Rochester. The registered enrollment target is 200 participants, below the 301-participant average among 154 other PTSD trials with a reported enrollment target (34% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06956781, a NA study of PTSD and Trauma, is actively recruiting participants, sponsored by University of Rochester.

RECRUITING
Registry status
NA
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to test the extent to which different treatment components work to improve pediatric post-traumatic stress disorder (PTSD). It will also provide evidence for how these components work. The main research questions are: What are the effects of different components used to treat PTSD? What do these components change to produce benefits in PTSD? Researchers will: Compare components to a psychological placebo to estimate their effects and measure how they work Examine how components work alone and in conjunction with other components Participants will: Receive different combinations of components and placebo Attend weekly treatment sessions Provide information to evaluate changes in PTSD

Primary Outcome

The CAPS-CA is a clinician-administered diagnostic interview measuring the severity of PTSD symptoms in the past month. The interview assesses 20 PTSD symptoms according to DSM-5 diagnostic criteria with each symptom rated on a severity scale ranging from 0 to 4. Ratings for each individual symptom are summed with higher scores indicating greater severities of PTSD symptoms (total scores range from 0-80).

Interventions

  • BEHAVIORAL Emotion Regulation
  • BEHAVIORAL Exposure
  • BEHAVIORAL Cognitive Processing
  • BEHAVIORAL Bi-lateral Stimulation
  • BEHAVIORAL Psychological Placebo

Study Locations (1)

New York

  • The Mt. Hope Family Center - Rochester

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2026-01
Est. Completion 2028-08
Phase NA
University of Rochester

636 total trials

What NCT06956781 shows while recruiting

NCT06956781 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 301-participant average among 154 other PTSD trials with a reported enrollment target (34% lower).

The record links to 3 conditions, with PTSD appearing as the primary indexed condition, and to 5 interventions - of which Emotion Regulation is the first listed.

NCT06956781 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT06956781 about?

NCT06956781 is a clinical study titled "Multiphase Optimization Strategy (MOST) for Treating Pediatric Post-traumatic Stress Disorder (PTSD)". The goal of this clinical trial is to test the extent to which different treatment components work to improve pediatric post-traumatic stress disorder (PTSD). It will also provide evidence for how these components work. The main research questions are: What are the effects of different components u...

What is the current status of trial NCT06956781?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2026-01. Estimated completion is 2028-08.

What conditions does trial NCT06956781 study?

This clinical trial studies the following conditions: PTSD, Trauma, Pediatric ALL.

What interventions are being tested in trial NCT06956781?

The interventions under investigation include: Emotion Regulation (BEHAVIORAL), Exposure (BEHAVIORAL), Cognitive Processing (BEHAVIORAL), Bi-lateral Stimulation (BEHAVIORAL), Psychological Placebo (BEHAVIORAL).

Who is sponsoring clinical trial NCT06956781?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06956781 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for PTSD

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06956781's enrollment target sits among peer trials

200 28th of 154 higher than 126 of 154 other PTSD trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other PTSD trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06956781, the US trial registry maintained by the National Library of Medicine. NCT06956781 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.