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Search / Trial NCT06628973

Social Prescribing to Improve Adherence and Outcomes in Women With Heart Failure

Launched by MCGILL UNIVERSITY HEALTH CENTRE/RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE · Oct 3, 2024

Trial Information

Current as of July 22, 2025

Not yet recruiting

Keywords

Heart Failure Social Determinants Of Health Adherence Social Prescribing Hospitalizations Readmissions Sex Gender Quality Of Life Congestive Heart Failure Women

ClinConnect Summary

This clinical trial is studying a new approach called "social prescribing" to help women with heart failure stick to their medication and improve their quality of life. Heart failure is a serious condition that affects many women, leading to frequent hospital visits and even death. Unfortunately, many women struggle to follow their medication plans, which can worsen their health. The trial aims to see if connecting these women with community resources and support based on their specific social needs—like help with transportation or mental health services—can lead to better medication adherence and overall well-being.

To participate in this trial, women must be 18 years or older, have a documented diagnosis of heart failure, and score two or more points on a specific questionnaire that identifies social challenges. Participants will be randomly assigned to either receive social prescribing support or standard care from their healthcare team. Those in the social prescribing group will work with a link worker who will help them access tailored services to meet their needs. The trial is not yet recruiting but aims to make a significant impact on the health of women with heart failure by addressing the factors that make it difficult for them to manage their condition.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Women
  • 18 years of age or older
  • Documented HF of any etiology
  • Valid personal health identifier
  • Two or more points on the weighted SPARK questionnaire
  • Exclusion Criteria:
  • Patients not meeting inclusion criteria
  • Do not take HF medications
  • Not residents of the province where they are being followed or who have opted out from their provincial health registry
  • Patients with severe cognitive impairment or other conditions that significantly impact the ability to participate in SP will also be excluded.

About Mcgill University Health Centre/Research Institute Of The Mcgill University Health Centre

The McGill University Health Centre (MUHC) and the Research Institute of the McGill University Health Centre (RI-MUHC) are leading institutions in clinical research and healthcare innovation. With a commitment to advancing medical knowledge and improving patient outcomes, the MUHC integrates cutting-edge research with high-quality patient care. The RI-MUHC fosters a collaborative environment where multidisciplinary teams engage in transformative research across various fields, including oncology, neurology, and cardiovascular health. By leveraging state-of-the-art facilities and a robust network of clinical expertise, both entities strive to translate scientific discoveries into effective treatments, ultimately enhancing the quality of life for patients locally and globally.

Locations

Montreal, Quebec, Canada

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported