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iParent2Parent Program for Parents of Children With Juvenile Idiopathic Arthritis (iPa2PaJIA)

T

The Hospital for Sick Children

Status

Completed

Conditions

JIA

Treatments

Behavioral: Waitlist Control
Behavioral: iParent2Parent Program

Study type

Interventional

Funder types

Other

Identifiers

NCT04168034
1000061063

Details and patient eligibility

About

The iParent2Parent program matches parents of children living with arthritis with a trained parent mentor who will provide parents of children newly diagnosed with arthritis: practical coping advice and social support through shared lived experiences. This study will compare two groups of parents: those who are in the iParent2Parent program and those in the control group (no mentor).

Full description

Parents/primary caregiver of children with JIA are an often overlooked but essential member of their child's health care team. They are responsible for managing their child's treatment program, and act as advocates for their child to support positive adaptation to JIA and to learn self-management skills for the disease. This is in the context of managing the financial, logistical, emotional, and social demands of parenting in general. Within pediatric tertiary care centres, peer-support programs for parents of children with JIA are often limited or difficult to access. The iParent2Parent Program aims to fill this gap in services by offering a program of trained parent peer mentors who can provide practical coping advice, foster adaptive problem solving, and provide social support via shared lived experience.

Enrollment

6 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English speaking caregiver of a child diagnosed with JIA according to ILAR criteria prior to their 18th birthday
  • Access to computer capable of using free Skype software

Exclusion criteria

  • Significant cognitive impairment or major co-morbid illness of parent that impeded ability to engage in program (e.g.; psychosis, active suicidal ideation, cognitive delays that would impact ability to participate and complete questionnaires.)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

6 participants in 2 patient groups

Experimental: iParent2Parent Mentorship
Experimental group
Description:
10 sessions of 20-30 minute Skype video calls conducted over 2 to 3 months
Treatment:
Behavioral: iParent2Parent Program
Waitlist Control Group
Active Comparator group
Description:
The control group will receive standard care but without the iParent2Parent program
Treatment:
Behavioral: Waitlist Control

Trial documents
2

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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