New therapy shows promise for healing war wounds in rwanda
NCT ID NCT07621731
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a type of group therapy called Resilience-Oriented Therapy (RoT) for adults in Rwanda who were struggling with mental health issues like trauma, depression, anxiety, or anger. 427 people took part, and the therapy was tailored to each person's main problem, such as managing emotions or behavior. The goal was to see if the therapy could help reduce symptoms and improve well-being.
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
-
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
-
427 people
The number who actually took part.
- Started
-
Apr 2023
- Finished
-
Sep 2023
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Adult participant aged 18 years or older. * Living in or connected to a selected RoT-eligible cluster in one of the five study districts in Rwanda. * Screened through the wider societal-healing screening process and assigned to one of the RoT variant pathways based on presenting mental-health or socioemotional profile. * Able and willing to complete baseline assessment and, if allocated to immediate RoT, participate in group sessions. * Written informed consent obtained according to local ethics requirements. Exclusion Criteria: * Acute clinical risk, including suicidality or other indication requiring more intensive clinical or hospital referral as first-line response. * Primary needs better matched to another intervention pathway after staged screening, including family-level healing or community sociotherapy. * Unable to provide informed consent or safely participate in group sessions.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Aggression are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
Contacts and locations
Locations
-
Community and Health-Centre Settings, Musanze District
Ruhengeri, Northern Province, Rwanda
-
Community and Health-Centre Settings, Ngoma District
Ngoma, Eastern Province, Rwanda
-
Community and Health-Centre Settings, Nyabihu District
Nyabihu, Western Province, Rwanda
-
Community and Health-Centre Settings, Nyagatare District
Nyagatare, Eastern Province, Rwanda
-
Community and Health-Centre Settings, Nyamagabe District
Nyamagabe, Southern Province, Rwanda
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Reading the Brain's signals to predict who benefits from deep brain stimulation
- Five sessions to quiet trauma nightmares in bipolar disorder
- Can practicing parenting in virtual reality calm Kids' aggression?
- Can a phone app that blocks distracting apps ease depression?
- Can video games calm anxious teens?
- Can teachers and a phone app ease teen depression?