Skip to content

iP2P Mentorship Program for Adolescent HF Patients

Implementation and Preliminary Effectiveness Evaluation of the iPeer2Peer Support Mentorship Program for Adolescent and Transitioning Heart Function Patients

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05709132
Acronym
iP2P HF
Enrollment
55
Registered
2023-02-01
Start date
2024-01-01
Completion date
2027-04-13
Last updated
2025-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Peer Support Mentorship, Pediatrics, Adherence, Cardiomyopathy

Brief summary

The iPeer2Peer (iP2P) program is an online peer support mentorship program that provides modelling and reinforcement by trained young adult peer mentors to adolescent mentees with the same condition. A quasi-experimental single-arm pre-post study design will be employed across three sites. We will recruit 40 mentees (12-17 years of age) and 12-15 mentors (18-30 years of age) who will undergo training in mentoring and the use of eHealth technology. Mentor-mentee pairings will connect over 15 weeks through video calls and text messaging to provide peer support and encourage disease self-management skills. Data will be collected using standardized instruments and interviews across three time points.

Interventions

Behavioral: iPeer2Peer Support Mentorship Program is an online peer support mentorship program that has been established in multiple chronic disease populations as a self-management intervention, including chronic pain and juvenile idiopathic arthritis. The iPeer2Peer program provides modeling and reinforcement by pre-screened and trained young adult peer mentors to adolescent mentees.

Sponsors

The Centre Hospitalier Universitaire Sainte-Justine
CollaboratorUNKNOWN
University of Alberta/Stollery Children's Hospital
CollaboratorUNKNOWN
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Quasi-experimental single arm pre-post study

Eligibility

Sex/Gender
ALL
Age
12 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

Mentee inclusion criteria: 1. patient with a cardiac diagnosis, 2. at least 4 months post-diagnosis, 3. between the ages of 12 and 17 years, 4. able to speak and read English, and 5. willingness to commit to 5-10 texts and/or calls of 20-30 minutes each with a peer mentor over a period of 15 weeks. Mentor inclusion criteria: 1. patient with a cardiac diagnosis, 2. between the ages of 18 and 30 years, 3. able to speak and read English, 4. nominated by a member of their health care team as a good mentor based on maturity and emotional stability, 5. willingness to commit to peer mentor training (20 hours) via the PHIPA-compliant version of Zoom or Microsoft Teams and mentoring adolescent participants (once paired with mentee, 5-10 texts and/or calls of 20-30 minutes over a period of 15 weeks), 6. good communication skills (as assessed by a healthcare provider), and 7. previous experience in a professional environment (e.g., as a camp counsellor, part time job, volunteering) is an asset.

Exclusion criteria

1. significant cognitive impairments as assessed by a qualified healthcare provider, 2. a diagnosis of an active psychological disorder (e.g., Major Depressive Disorder, Generalized Anxiety Disorder) likely to influence assessment of health-related quality of life and/or interfere with their ability to manage their heart failure care regimen (a diagnosis of an active psychological disorder will be determined for mentees through medical chart review and self-reported by mentors), and 3. participating in other peer support or self-management interventions.

Design outcomes

Primary

MeasureTime frameDescription
Level of engagement (Mentors)Study completion, an average of 1 year
Acceptability (Mentees)15 weeks after baseline/immediately after the interventionWhether the innovation is agreeable, palatable or satisfactory
Acceptability (Mentors)Study completion, an average of 1 yearWhether the innovation is agreeable, palatable or satisfactory
Adoption (Mentees)Baseline to 12 weeks post-program completionThe intention, initial decision or action to try or use an innovation
Adoption (Mentors)Baseline to study completion, an average of 1 yearThe intention, initial decision or action to try or use an innovation
Feasibility (Mentees)Baseline to 12 weeks post-program completionThe extent to which an innovation can be used or carried out successfully in a given setting
Feasibility (Mentors)Baseline to study completion, an average of 1 yearThe extent to which an innovation can be used or carried out successfully in a given setting
Appropriateness (Mentees)Baseline to 12 weeks post-program completionThe perceived fit, relevance or compatibility of the innovation for a practice setting; and/or its perceived fit to address an issue or problem
Appropriateness (Mentors)Baseline to study completion, an average of 1 yearThe perceived fit, relevance or compatibility of the innovation for a practice setting; and/or its perceived fit to address an issue or problem
Level of engagement (Mentees)15 weeks after baseline/immediately after the intervention

Secondary

MeasureTime frameDescription
Perceived social role satisfaction (Mentors)Baseline to study completion, an average of 1 year
Self-efficacy (Mentors)Baseline to study completion, an average of 1 year
Quality of life (Mentees)Baseline to 12 weeks post-program completion
Perceived social support (Mentees)Baseline to 12 weeks post-program completion
Emotional distress (Mentees)Baseline to 12 weeks post-program completion
Resiliency (Mentees)Baseline to 12 weeks post-program completion
Assessment of mentor quality (Mentees)15 weeks after baseline/immediately after the intervention
Physical and emotional symptoms (Mentors)Baseline to study completion, an average of 1 year
Disease self-management skills (Mentees)Baseline to 12 weeks post-program completion
Adherence (Mentees)Baseline to 12 weeks post-program completionClinic attendance, completion of scheduled tests and procedures, and adolescent medication barriers scale

Countries

Canada

Contacts

Primary ContactSamantha J Anthony, PhD
samantha.anthony@sickkids.ca416-813-7654
Backup ContactSophie Bui, BHSc
sophie.bui@sickkids.ca

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026