Skip to main content
Clinical Trials/NCT01054963
NCT01054963CompletedNot Applicable

Peer to Peer Mentoring: Facilitating Individuals With Early Inflammatory Arthritis to Manage Their Arthritis - Peer Mentor Training

Sunnybrook Health Sciences Centre1 site in 1 country10 target enrollmentStarted: January 1, 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
ability to provide informational, appraisal and emotional support

Study Overview

Brief Summary

Inflammatory arthritis (IA) is a major cause of long-term disability. Peer support may be a solution to the common problem of delayed treatment. Early peer support may result in improved use of therapy, higher self-efficacy, reduced anxiety, and improved coping in the first two years post-diagnosis. This study involves the development and testing of a peer mentor training initiative as one part of an intervention study for people with early IA (EIA). Peer mentors will be trained and assessed to provide one-on-one support (information, emotional, feedback) to individuals who have recently been diagnosed with IA. This is one part of an intervention study. The other part is called Peer to Peer Mentoring: Facilitating Individuals with Early Inflammatory Arthritis to Manage their Arthritis - Peer Mentoring Program.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Supportive Care

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • To become a peer mentor are:
  • Diagnosis of IA from a physician
  • Disease duration more than 2 years and managing well
  • Currently using medications (DMARDS/biologics) to treat arthritis
  • Have completed an Arthritis Self-Management Program (ASMP) provided by The Arthritis Society and/or similar program and/or have sufficient knowledge and experience with teaching or providing mentoring support to an individual living with a chronic disease
  • Able to participate in two approximately 5-hour training workshops
  • Able to take part in ongoing assessment/evaluation activities (self-report questionnaire, interviews, observation, study activity log)
  • Able to commit to the duration of the research study
  • Willing to provide ongoing one-on-one support to an individual newly diagnosed with IA
  • 18 years of age or older
  • Able to speak, understand, read and write English

Exclusion Criteria

  • Do not meet inclusion criteria

Outcomes

Primary Outcomes

ability to provide informational, appraisal and emotional support

Time Frame: 0, 3, 6 months

Secondary Outcomes

  • confidence to provide informational, appraisal and emotional support(0, 3, 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Mary Bell

Rheumatologist

Sunnybrook Health Sciences Centre

Study Sites (1)

Loading locations...

Similar Trials