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Behavioral Intervention

Mantram repetition program for Post-Traumatic Stress Disorder

N/A
Recruiting
Led By Ahmed Hassan, MD, MPH
Research Sponsored by Centre for Addiction and Mental Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline; week 4; week 8; week 12 follow up. scale title: 12-item short form health survey , minimum value: 0 , maximum value : 100. the higher the score the better the outcome.
Awards & highlights

Study Summary

This trial will help evaluate if a program involving the repeated spiritual phrase can help those with PTSD and substance abuse disorders.

Eligible Conditions
  • Post-Traumatic Stress Disorder
  • Substance Use Disorder

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline; week 4; week 8; week 12 follow up. scale title: 12-item short form health survey , minimum value: 0 , maximum value : 100. the higher the score the better the outcome.
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline; week 4; week 8; week 12 follow up. scale title: 12-item short form health survey , minimum value: 0 , maximum value : 100. the higher the score the better the outcome. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Rate of retention in the group
Secondary outcome measures
Alcohol consumption
CAPS-5 PTSD Symptom Severity (past month)
Drug consumption
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Mantram repetition programExperimental Treatment1 Intervention
Weekly 90 minute virtual group therapy sessions for 8 weeks run by two faciliators and will consist of 5-8 participants.

Find a Location

Who is running the clinical trial?

Centre for Addiction and Mental HealthLead Sponsor
355 Previous Clinical Trials
81,184 Total Patients Enrolled
Ahmed Hassan, MD, MPHPrincipal InvestigatorCentre for Addiction and Mental Health

Media Library

Virtual Mantram Program (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05058963 — N/A
Post-Traumatic Stress Disorder Research Study Groups: Mantram repetition program
Post-Traumatic Stress Disorder Clinical Trial 2023: Virtual Mantram Program Highlights & Side Effects. Trial Name: NCT05058963 — N/A
Virtual Mantram Program (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05058963 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the total size of the patient population included in this research?

"Affirmative. As indicated on clinicaltrials.gov, this medical study is still recruiting patients and began enlisting volunteers as of May 1st 2021. With one labelled site, the trial seeks to enrol 60 participants in total."

Answered by AI

Are there still recruitment opportunities for participants in this trial?

"According to the clinicaltrials.gov database, this medical experiment is actively seeking out participants. It was initially published on May 1st 2021 and revised as recently as September 16th 2021."

Answered by AI

Who else is applying?

What state do they live in?
Ontario
North Carolina
How old are they?
18 - 65
What portion of applicants met pre-screening criteria?
Did not meet criteria
Met criteria
What site did they apply to?
Centre for Addiction and Mental Health
How many prior treatments have patients received?
0

How responsive is this trial?

Typically responds via
Email
Most responsive sites:
  1. Centre for Addiction and Mental Health: < 24 hours
Average response time
  • < 1 Day
Recent research and studies
clinicaltrials.govStudy
Virtual Mantram Program for Patients With PTSD and SUD
2021. "Virtual Mantram Program for Patients With PTSD and SUD". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05058963.
~15 spots leftby Apr 2025
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