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CompletedNCT01054131Updated Dec 29, 2011

Peer to Peer Mentoring: Facilitating Individuals With Early Inflammatory Arthritis to Manage Their Arthritis: Peer Mentoring Program

An interventional study of peer support in Early Inflammatory Arthritis and Chronic Disease, sponsored by Sunnybrook Health Sciences Centre. Completed at 1 site in Canada. Per ClinicalTrials.gov, last updated 2011-12-29.

Sponsored by Sunnybrook Health Sciences Centre · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Sex
All
01

Study 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. The whole intervention study comprises of two parts: The first part involves the development and testing of a peer mentor training initiative, which is called "Peer to Peer Mentoring: Facilitating Individuals with Early Inflammatory Arthritis to Manage their Arthritis - Peer Mentor Training". The second part, which is the focus of this study, involves the delivery of a one-on-one peer support intervention from a trained peer mentor to an individual newly diagnosed with EIA. The feasibility and acceptability of the program will be determined, as well as the health outcomes following the participation of the program.

02

Conditions studied

  • Early Inflammatory Arthritis
  • Chronic Disease

Keywords

  • peer support
  • peer mentor
  • self-management
  • early inflammatory arthritis
  • chronic disease
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In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 317 are open to participants now.

This study's planned enrollment of 10 is below the median of 90 across 2,377 interventional studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

Sunnybrook Health Sciences Centre is the lead sponsor of 566 studies on the registry; 134 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Have EIA disease duration within 6-52 weeks
  2. At least 3 swollen joints, assessed by the treating rheumatologist, OR positive compression test for the metacarpophalangeal joints OR positive compression test for the metatarsophalangeal joints OR at least 30 minutes of morning stiffness
  3. Prescription of a DMARD/biologic by the treating rheumatologist
  4. Ability to speak and understand English without the aid of a secondary support person; AND
  5. Capability to provide informed consent.

Exclusion criteria

Exclusion Criteria:

  1. IA disease duration less than 6 weeks or greater than 1 year
  2. Previous or ongoing DMARD or biologic treatment
  3. Inability to speak or read grade 6 English; AND
  4. Inability to provide informed consent
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Enrollment
10 participants (estimated)

Interventions

  • Behavioralpeer support

    A quasi-experimental, before and after study design will obtain data for planning and implementing a larger-scale study. Exposures and outcomes will be measured at baseline, 3 months (immediate post 12-week program) and 6 months (3 months post-program). Ten individuals with EIA will be recruited by brief screening interviews to ensure they meet inclusion criteria. Each pair of peer mentor and EIA participant will meet at SHSC for an initial contact. EIA participants will receive informational, emotional and appraisal support from trained peer mentors by telephone or neutral private location at a time convenient for both parties, at least once a week for 12 weeks.

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What researchers measure

Primary outcomes

  1. DMARD adherence

    Time frame: 0, 3, 6 months

Secondary outcomes

  1. coping efficacy

    Time frame: 0, 3 6 months

  2. self-management

    Time frame: 0, 3, 6 months

  3. anxiety

    Time frame: 0, 3, 6 months

  4. self efficacy

    Time frame: 0, 3, 6 months

  5. social support

    Time frame: 0, 3, 6 months

07

Study locations

1 site
  • Sunnybrook Health Sciences Centre
    Toronto, Ontario, Canada
08

References and documents

Publications

  • Sandhu S, Veinot P, Embuldeniya G, Brooks S, Sale J, Huang S, Zhao A, Richards D, Bell MJ. Peer-to-peer mentoring for individuals with early inflammatory arthritis: feasibility pilot. BMJ Open. 2013 Mar 1;3(3):e002267. doi: 10.1136/bmjopen-2012-002267. PubMed 23457326 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 29, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01054131
Lead sponsor
Sunnybrook Health Sciences Centre
Collaborators
Canadian Arthritis Network
Responsible party
Dr. Mary Bell (Rheumatologist, Sunnybrook Health Sciences Centre) — Principal investigator
First posted
Jan 22, 2010
Start date
Jan 2010
Primary completion
Sep 2011
Completion
Dec 2011
Last update
Dec 29, 2011

Study contacts

Mary J Bell, MD, FRCPC
principal investigator · Rheumatologist, Sunnybrook Health Sciences Centre

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2011. You cannot join it, but the record below documents what was studied.

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