Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06651801

A Pilot Randomized Controlled Trial Assessing the Feasibility and Acceptability of Group Medical Visits for Anxiety and Depression

Led by University of Manitoba · Updated on 2025-05-13

20

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying Group Medical Visits (GMVs) to see if they are practical and well-received by adults with depression and anxiety. This pilot randomized controlled trial aims to gather early information on whether GMVs can reduce depression and anxiety symptoms, which will help design a larger future study. The main focus is to find out if patients find GMVs feasible and acceptable as part of their mental health care. Participants are randomly placed into one of two groups: one receives GMVs every two weeks for six months via virtual meetings, where they participate in group discussions, psychoeducation, and medication follow-ups, including brief individual check-ins. The other group receives standard care, which includes follow-up with their primary care provider, possible individual psychiatric care, and referrals to therapy groups if needed. Throughout the study, participants will complete questionnaires evaluating satisfaction with care, depression and anxiety levels, recovery, and quality of life at different points, including before and during the intervention at months 3 and 6. The study will also track recruitment, retention, and satisfaction of primary care providers. Participation involves virtual sessions and assessments over approximately nine months, with safety and effectiveness monitored throughout.

CONDITIONS

Brief Title

Feasibility and Acceptability of Group Medical Visits for Anxiety and Depression

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult Central Intake patients referred for psychiatric consultation whose main mental health issue is an anxiety disorder (social anxiety, generalized anxiety, or panic disorder) or depression (major depressive disorder or persistent depressive disorder)
  • Able to participate in an English language virtual group with up to 10 participants
  • Able to commit to biweekly virtual groups lasting about 1.5 hours each
  • Able to join virtual groups from a private location with camera access
  • Live in the community in Manitoba and plan to stay for the 6-month study period
Not Eligible

You will not qualify if you...

  • Diagnosis of Bipolar 1 or 2 Disorder
  • Primary diagnosis of a personality disorder causing anxiety or depression symptoms
  • Already receiving ongoing care from a psychiatrist
  • Received electroconvulsive therapy (ECT) within the past 6 months
  • Any diagnosis significantly impacting ability to participate, including moderate-to-severe substance use disorder, current psychotic symptoms, moderate-to-severe intellectual disability or neurocognitive disorder
  • Significant eating disorder symptoms causing major physical or mental impact
  • Self-harm requiring medical or psychiatric attention or active suicidal thoughts or attempts within past 6 months
  • Safety concerns for other group members or facilitators if participant joins the group

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (virtual)

Outpatient Treatment

Duration - 6 months

Participants in the experimental group attend biweekly virtual group medical visits involving psychoeducation, group support, and medication follow-up. Participants in the control group follow up with their primary care provider as usual.

Group medical visits every 2 weeks virtually (via Zoom), each lasting about 1.5 hours including individual check-ins

Trial Site Locations

Total: 1 location

1

PsycHealth Centre

Winnipeg, Manitoba, Canada, R3E 3N4

Actively Recruiting

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Research Team

K

Kirsten Penner-Goeke, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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Frequently Asked Questions

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Published Research Related To This Trial

A protocol paper for a pilot randomized controlled trial assessing the feasibility and acceptability of group medical visits for anxiety and depression in adults.

Christian Kordan, Jennifer Hensel, Jitender Sareen...

https://pubmed.ncbi.nlm.nih.gov/42050722