Cardiac Rehabilitation Peer Mentorship
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|ClinicalTrials.gov Identifier: NCT02204449|
Recruitment Status : Completed
First Posted : July 30, 2014
Results First Posted : June 22, 2015
Last Update Posted : December 30, 2015
|Condition or disease||Intervention/treatment||Phase|
|Percutaneous Coronary Intervention Coronary Artery Bypass Graft Surgery, With or Without Valve Surgery Acute Coronary Syndrome Chronic Stable Heart Failure Coronary Artery Disease||Behavioral: Cardiac Rehabilitation Peer Mentorship||Not Applicable|
The current study will be a randomized controlled trial in which cardiac inpatients will be randomized to either receive the intervention (cardiac rehabilitation peer mentorship) or be in the control group (receive usual care). After consent is obtained cardiac patients in the intervention group will be visited, at the hospital bedside, by trained volunteer cardiac rehabilitation peer mentors (i.e., individuals who have completed cardiac rehabilitation) who will provide the patients with information on cardiac rehabilitation as well as encourage the patients to obtain a referral from their healthcare provider. During this visit the cardiac rehabilitation peer mentor will also obtain agreement from the patient to call the patient at home two weeks after their discharge. Those in the control group will not be visited by cardiac rehabilitation peer mentors.
One week after discharge the cardiac rehabilitation peer mentors will mail the patients in the intervention a get-well soon card reminding the patient of the visit, giving them more information about the cardiac rehabilitation program, and reminding them of their future scheduled phone call. Two weeks after patients' discharge cardiac rehabilitation peer mentors will call the patients in the intervention group. At this point they will assess how the patient is doing, if they were referred to cardiac rehabilitation and if they enrolled. Any possible barriers the patients have to attending cardiac rehabilitation will also be discussed.
Eight weeks post-discharge, patient referral and enrolment will be ascertained by a research assistant blinded to random assignment. Statistical analyses will be conducted to determine any differences between the two groups as well as to determine any differences between men and women.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||94 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Primary Purpose:||Health Services Research|
|Official Title:||Mentorship to Promote Cardiac Rehabilitation Enrollment: A Randomized Controlled Trial|
|Study Start Date :||July 2014|
|Actual Primary Completion Date :||January 2015|
|Actual Study Completion Date :||January 2015|
Experimental: Cardiac Rehabilitation Peer Mentorship
Trained cardiac rehabilitation (CR) peer mentors will visit cardiac inpatients in the hospital to provide patients with information on CR. During this visit the CR mentors will discuss the benefits of CR, stress the importance of getting a referral, and arrange a time to call the patient/participant at home to find out about their CR progress. One week post-discharge the peer mentor will mail a card to the patient to remind them of the planned call. Two weeks post-discharge the peer mentor will call the patient at home to determine if they were referred and if they are planning to attend CR. If any barriers are stated by patient the peer mentors will work with the patient to develop possible solutions. Patients can request up to two additional phone calls from the mentors.
Behavioral: Cardiac Rehabilitation Peer Mentorship
No Intervention: Usual Care
Cardiac inpatients will not be visited by the cardiac rehabilitation (CR) peer mentor. They will instead receive usual care involving care from health care providers (i.e. nurses and doctors) as well as allied health professionals such as physiotherapists. In addition, some may be visited by general volunteer cardiac mentors.
- Cardiac Rehabilitation Enrollment [ Time Frame: 12 weeks after patient is discharged from hospital ]A blinded research assistant will either examine medical records or call the participant (i.e., patient) at home to determine if they have enrolled in cardiac rehabilitation.
- Cardiac Rehabilitation Referral [ Time Frame: 12 weeks after patient has been discharged from hospital ]A blinded research assistant will examine patient medical records to determine if patients were referred to cardiac rehabilitation.
- Cardiac Rehabilitation Enrollment in Site Closer to Home [ Time Frame: 8 weeks after patient is discharged from hospital ]A blinded research assistant will call those patients who were re-referred to a cardiac rehabilitation site closer to their home to see if they enrolled in cardiac rehabilitation. The study coordinator will then compare this to enrollment rates (already determined by the blinded research assistant) of those who enrolled in the program at the hospital system in which they were inpatients.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02204449
|Toronto General Hospital|
|Toronto, Ontario, Canada, M5G2C4|
|Toronto Western Hospital|
|Toronto, Ontario, Canada, M5T2S8|
|Principal Investigator:||Sherry Grace, PhD||York University|