Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Well-being program for caregivers of patients with advanced heart or lung disease

Official title: Enhancing Caregiver Wellbeing: The Role of Exercise, Nutrition, and Stress Management for Caregivers of Patients With Advanced Cardiac and Pulmonary Disease

Run by University Health Network, Toronto · NCT07685912 · Data updated 2026-11-12

This study tests an 8-week, home-based wellness program delivered virtually to caregivers of people with advanced cardiac or pulmonary disease to see if it’s feasible and acceptable.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorUniversity Health Network, Toronto
Academic / other
Locations1 site (Toronto, Ontario)
StatusRecruiting
StartedNovember 1, 2026
Main results expectedMarch 30, 2028
Study endsMarch 30, 2028
Registry record updatedNovember 5, 2026
Trial IDNCT07685912 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are informal caregivers aged 18 or older of patients with advanced cardiac or pulmonary disease receiving outpatient palliative care at Toronto General Hospital, who have internet access and can consent.

Probably not a fit

Patients who do not receive direct medical intervention may still benefit indirectly if caregiver well-being improves caregiving capacity, but individual patient benefit is not guaranteed.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study provides an 8-week multimodal wellness program delivered remotely to informal caregivers of patients with advanced cardiac or pulmonary disease. The program combines personalized exercise guidance, nutrition support, and stress management, with regular virtual check-ins from health professionals. Feasibility, safety, acceptability, and adherence will be assessed to determine if caregivers can participate and benefit in a home-based format. The study is conducted at Toronto General Hospital, led by University Health Network, focusing on caregiver well-being alongside potential impacts on caregiving capacity.

Why it matters

Potential benefit: If successful, caregivers may experience improved stress management, physical activity, nutrition habits, and overall well-being, with potential downstream benefits for patient care.

How similar studies have gone: Prior virtual wellness programs in similar populations have shown feasibility and safety, supporting potential success for this caregiver-focused approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
INCLUSION CRITERIA (CAREGIVERS):

* Informal (unpaid) caregivers aged 18 years or older
* Identified as the primary caregiver of a patient with advanced cardiac or pulmonary disease receiving outpatient palliative care at Toronto General Hospital
* Ability to provide informed consent

EXCLUSION CRITERIA (CAREGIVERS):

* Presence of any medical condition where moderate physical activity or exercise training would be contraindicated (e.g., unstable cardiovascular disease, recent injury)
* Significant cognitive impairment or language barrier that would interfere with completing study procedures
* Lack of access to a phone or internet connection to enable virtual participation

INCLUSION CRITERIA (Patients):

* Aged 18 years or older
* Diagnosis of advanced cardiac or pulmonary disease and currently receiving outpatient palliative care at Toronto General Hospital
* Ability to provide informed consent

EXCLUSION CRITERIA (Patients):

* Significant cognitive impairment or language barrier that would interfere with completing study procedures
* Medical instability that would preclude participation in an interview or completion of questionnaires, as determined by the clinical team
* Lack of access to a phone or internet connection to enable virtual participation

Where it's running

  • University Health Network
    Toronto, Ontario, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.