TAG TEAM: Group CBT for minority stress in trans and gender diverse teens
Official title: Evaluation of Trans Adolescent Group ThErapy for Alleviating Minority Stress (TAG TEAM): a Randomised Controlled Trial
Run by Murdoch Childrens Research Institute · NCT07151079 · Data updated 2026-11-12
This trial tests a group CBT program to help trans and gender diverse adolescents cope with minority stress and improve mood and wellbeing.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 17 Years |
| Sex | All |
| Enrollment | 142 (estimated) |
| Sponsor | Murdoch Childrens Research Institute Academic / other |
| Locations | 1 site (Parkville, Victoria) |
| Status | Recruiting |
| Started | May 21, 2026 |
| Main results expected | November 2026 |
| Study ends | March 2027 |
| Registry record updated | June 5, 2026 |
| Trial ID | NCT07151079 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are trans, non-binary, or gender-diverse adolescents aged 12-17 with moderate or higher psychological distress who can provide informed consent along with a guardian.
✕Probably not a fit
Participants who do not experience reductions in distress or who prefer individual therapy may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares the TAG TEAM group CBT program to a waitlist control in trans and gender diverse youths aged 12-17 with moderate or higher psychological distress. The 6 weekly, 2-hour sessions cover minority stress, protective factors, and coping skills, with videos and discussions led by a psychologist and a trans peer facilitator. A mixed-methods design includes quantitative outcomes and a qualitative sub-study using photovoice or interviews to explore participant experiences. The study builds on co-design with the community to assess feasibility, acceptability, and effectiveness. Sessions include a mid-session break and between-session activities consistent with core CBT principles.
Why it matters
Potential benefit: If successful, participants may experience reduced distress and improved wellbeing and coping related to minority stress.
How similar studies have gone: Previous group CBT approaches for minority stress in transgender youth have shown promise, but this program is co-designed with the community and includes a unique photovoice qualitative component.
Who can join: the full rules
Show full inclusion / exclusion criteria
Participants will be enrolled into the RCT only if they meet all the inclusion criteria and none of the exclusion criteria. Inclusion Criteria: * Identifies as trans, non-binary, or gender diverse * Is between the ages of 12 and 17 years inclusive * Has completed primary school at the time of enrolment into the study * Has current psychological stress symptomology as determined by a score of moderate or above on the DASS-Y * Provide informed consent: All participants and parent/legal guardians must be willing to give informed consent Exclusion Criteria: * Has current acute suicidal symptomology as determined by a combination of clinical judgement and the results of the Ask Suicide-Screening Questions (ASQ) suicide screening tool (e.g., answer yes to question 5) to determine the risk of suicide (has an active plan and/or intent to suicide) at time of screening interview * Is actively having treatment with any other group psychological intervention at the time of enrolment into the study * Is not proficient in English (as the group Cognitive behaviour therapy (CBT) program will be delivered in English and funds aren't available for interpreters) * Previous participation in the feasibility trial * Is currently enrolled in tertiary study (e.g., undergraduate university)
Where it's running
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Murdoch Children's Research Institute
Parkville, Victoria, Australia Recruiting
Study contacts
- Principal investigator: Timothy J Cronin, PhD — Murdoch Childrens Research Institute
- Study coordinator: Timothy J Cronin, PhD
- Email: tagteam@mcri.edu.au
- Phone: +61393456991
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.