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Behavioural Intervention

single arm for Post-Traumatic Stress Disorder (NM Trial)

N/A
Waitlist Available
Led By Edward F Pace-Schott, PhD
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 24 weeks.
Awards & highlights

NM Trial Summary

This trial is looking for people with PTSD who will complete a series of interviews and tests, including sleep and nightmare diaries and questionnaires, to see if a new treatment called SDI is effective.

Eligible Conditions
  • Post-Traumatic Stress Disorder

NM Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after the procedure.
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately after the procedure. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
fNIRS rlIFG difference score
psychophysiological difference score
Secondary outcome measures
fNIRS difference score for remaining 7 frontolateral ROIs

NM Trial Design

1Treatment groups
Experimental Treatment
Group I: single armExperimental Treatment1 Intervention
entirely within-subject outcome variables

Find a Location

Who is running the clinical trial?

Massachusetts General HospitalLead Sponsor
2,931 Previous Clinical Trials
13,198,415 Total Patients Enrolled
Edward F Pace-Schott, PhDPrincipal InvestigatorMass General Brigham
1 Previous Clinical Trials
52 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~6 spots leftby Apr 2025