Could a trusted friend or family member enhance PTSD recovery?
NCT ID NCT07797543
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This study tests whether adding a support person to a trauma-informed cognitive training program helps people with post-traumatic stress improve their daily functioning and reduce distress. The program, called TIGMT, teaches skills like attention, planning, and problem-solving, adapted for people who have experienced trauma. Half of the participants will also bring a trusted adult to three extra sessions to learn how to reinforce these skills at home. Researchers will compare the two groups to see if the support person module improves engagement, symptoms, and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Trauma-Informed Goal Management Training (TIGMT) with an added Support-Person Module
- What this could lead to
- If it works, this could point toward a more effective way to help people with post-traumatic stress improve their thinking skills and daily functioning by involving a trusted support person.
- What could go wrong
- This is a small pilot study, so results may not apply to everyone. Adding a support person may not improve outcomes, and the extra sessions could be burdensome for some participants.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * be able to read, write, and speak English fluently * reside in Ontario * be able to provide written informed consent * be between the ages of 18 and 65 (to ensure generalizable results) * meet screening criteria for PTSD or Complex-PTSD (CPTSD) on the ITQ, administered at the time of screening, to be corroborated with the results of the ITI * be able to attend regular online, 2-hour sessions once/week for 9 weeks, and be willing to complete the pre-, post-intervention, and follow-up assessments * have reliable access to a computer with a working microphone and camera, and * have reliable and consistent access to the internet. Exclusion Criteria: * use benzodiazepines daily or almost daily * use narcotics daily or almost daily * meet criteria for Alcohol/Cannabis use that may interfere with their ability to participate in the study, as assessed by the AUDIT and CUDIT-R embedded into the eligibility pre-screener and corroborated with the DART (to be determined by the clinical team) * have a history of Moderate to Severe brain injury or loss of consciousness with prolonged effects that interfere with daily functioning at school, work, or within the family unit * have a history of a neurological disorder that may interfere with their ability to participate in the study (to be determined by Dr. McKinnon's clinical team) * have a diagnosis of psychotic disorder, borderline personality disorder, or bipolar disorder * have a diagnosis of a neurodevelopmental disorder that may interfere with their ability to participate in the study (to be determined by Dr. McKinnon's clinical team) * have other conditions/impairments/considerations that could interfere with completion of study tasks or participation in the study (to be determined by Dr. McKinnon's clinical team) * have previously participated in GMT * are receiving treatment with anti-cholinergics, anti-psychotic medication, or psychostimulants * have had ECT within the past year * are currently engaged in a trauma-focused intervention that may confound the findings of the current study (to be determined by Dr. McKinnon's clinical team) * are an active serving member of the Canadian Armed Forces.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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McMaster University
Hamilton, Ontario, L9C 1G2, Canada
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