Actively Recruiting

Phase Not Applicable
Age: 55Years +
All Genders
Healthy Volunteers
ID07107906

The CONNECT Program: Engaging Community Organizations in Implementing and Evaluating a Group Telehealth Mental Health Program for Older Canadians

Led by University of Manitoba · Updated on 2025-09-19

128

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

U

University of Manitoba

Lead Sponsor

A

A & O: Support Services for Older Adults

Collaborating Sponsor

AI-Summary

What this Trial Is About

Older adults in Canada are facing growing challenges with social isolation, loneliness, anxiety, and depression, especially following the COVID-19 pandemic. These issues are linked to worse mental and physical health, higher dementia risk, and increased mortality. Social connection helps protect health and well-being, but many older adults do not access mental health services due to barriers. This research evaluates The CONNECT Program, a group-based telehealth intervention designed to reduce loneliness and mental health symptoms in adults aged 55 and older. The study compares The CONNECT Program, delivered via telephone or Zoom in six weekly 90-minute group sessions, to routine community participation programs offered in-person, by phone, or virtually. Participants will be randomly assigned to receive either The CONNECT Program first followed by usual community programming, or vice versa, each phase lasting six weeks. The CONNECT Program uses Acceptance and Commitment Therapy, self-compassion, and theories of successful aging, including structured workbooks and homework assignments. Participants will be assessed at baseline, after each 6-week phase, and at a 6-month follow-up. Researchers will measure changes in psychological flexibility, loneliness, social isolation, anxiety, depression, emotional support, and mental health literacy. The study also examines how well the program can be implemented in community settings. The total involvement includes participation in group sessions and completing questionnaires to track mental health and social outcomes over time.

CONDITIONS

Brief Title

Evaluating and Implementing The CONNECT Program - a Group-Based Telehealth Intervention to Reduce Social Isolation, Loneliness, and Mental Health Symptoms in Adults Ages 55+, Compared to Routine Community-Based Programming

Who Can Participate

Age: 55Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 55 years or older
  • Able to speak, read, and understand English
  • Can manage hearing or vision changes well enough to participate in group conversations
  • Self-reported experiences of loneliness, social isolation, and/or mental health challenges such as anxiety or depressive symptoms
Not Eligible

You will not qualify if you...

  • Cannot communicate in English, either verbally or in writing

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 (in-person or virtual)

Treatment

Duration - Two 6-week phases

Participants receive either The CONNECT Program or community-based programming as usual in a crossover design. The CONNECT Program is a group-based telehealth intervention with 6 weekly 90-minute sessions delivered by phone or Zoom. Community-based programming involves regular social, educational, or recreational group sessions offered by local organizations.

Weekly group sessions for 6 weeks in each phase

Follow-up

Duration - Up to 6 months after treatment completion

Participants complete assessments to measure changes in psychological flexibility, loneliness, social isolation, emotional support, anxiety, depression, and mental health literacy up to 6 months after treatment.

1 follow-up visit at 6 months

Trial Site Locations

Total: 1 location

1

University of Manitoba

Winnipeg, Manitoba, Canada, R3T 2M8

Actively Recruiting

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Research Team

K

Kristin AA Reynolds, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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Item banks for measuring emotional distress from the Patient-Reported Outcomes Measurement Information System (PROMIS®): depression, anxiety, and anger.

Paul A Pilkonis, Seung W Choi, Steven P Reise...

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Social support network structure in older people: underlying dimensions and association with psychological and physical health.

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From Social Integration to Social Isolation: The Relationship Between Social Network Types and Perceived Availability of Social Support in a National Sample of Older Canadians.

Oksana Harasemiw, Nancy Newall, Shahin Shooshtari...

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Preliminary psychometric properties of the Acceptance and Action Questionnaire-II: a revised measure of psychological inflexibility and experiential avoidance.

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https://pubmed.ncbi.nlm.nih.gov/22035996