Actively Recruiting

Phase Not Applicable
Age: 12Years - 18Years
All Genders
NCT05382962

iCanCope With Post-Operative Pain (iCanCope PostOp)

Led by The Hospital for Sick Children · Updated on 2025-07-09

60

Participants Needed

2

Research Sites

226 weeks

Total Duration

On this page

Sponsors

T

The Hospital for Sick Children

Lead Sponsor

B

Boston Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

There are few applications available in the community to help teenagers manage pain after surgery. The focus of this study is to better understand the pain experience of children after having surgery and to design a Smartphone app called "iCanCope with Post-Operative Pain" (iCanCope PostOp), to help children and parents to better manage pain at home after surgery. The app will help keep track of pain, provide information about the teenager's surgery and provides "in-the-moment" advice wherever and whenever the patient needs it.

CONDITIONS

Official Title

iCanCope With Post-Operative Pain (iCanCope PostOp)

Who Can Participate

Age: 12Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 12 to 18 years
  • Own a smartphone compatible with the iCanCope app (iOS or Android)
  • Diagnosed with adolescent idiopathic scoliosis, pectus carinatum, or pectus excavatum
  • Able to speak and read English
  • Scheduled for scoliosis or minimally invasive pectus repair surgery
Not Eligible

You will not qualify if you...

  • Significant cognitive impairment or medical condition limiting ability to use the app, as identified by a healthcare provider
  • Previous participation in a study of iCanCope PostOp
  • Diagnosed chronic pain condition unrelated to the surgical condition

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Boston Children's Hospital

Boston, Massachusetts, United States, 02115

Not Yet Recruiting

2

Hospital for Sick Children

Toronto, Ontario, Canada, M5G 1X8

Actively Recruiting

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Research Team

J

Jennifer Stinson, RN, PhD

CONTACT

C

Chitra Lalloo, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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