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iCanCope With Pain: A Smartphone and Web Self-management Program for Adolescents and Young Adults With Chronic Pain

T

The Hospital for Sick Children

Status

Completed

Conditions

Chronic Pain

Treatments

Behavioral: iCanCope app and website
Behavioral: Attention control group

Study type

Interventional

Funder types

Other

Identifiers

NCT02601755
1000047495

Details and patient eligibility

About

Chronic pain in adolescents and young adults (AYA, aged 15-25) is a common problem. Pain that is not treated properly can reduce quality of life. Programs to help AYA learn to live with and manage pain are very important. Our team is developing a smartphone application (app) and website for AYA with chronic pain. The app will help AYA to track pain, sleep, mood, activities, and exercise and help AYA set and achieve goals. The website will give information about pain and how to manage it independently. We will build the program and make sure it is easy to use and understand. We will also test if the program can be put into practice as planned and if AYA using the program feel less pain, have less limitations, and a better quality of life.

Enrollment

302 patients

Sex

All

Ages

15 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with chronic pain of at least 3 months duration according to medical chart
  • Able to speak and read English
  • Willing and able to complete online measures
  • Participants are active patients at pain clinic at one of the respective participating study sites
  • Have access to an Internet-connected computer according to self-report.

Exclusion criteria

  • Moderate to severe cognitive impairments, as assessed by reviewing medical chart and consultation with the patient's healthcare provider
  • Major co-morbid psychiatric (e.g. conversion disorder, depression, anxiety disorder) illness that may impact patient's ability to understand and use the iCanCope with Pain intervention via self-report, as determined by their health care provider
  • Patient from the department of haemology/oncology
  • Participated in the Phase 2B iCanCope usability study
  • Requires urgent CBT treatment as per their health care provider
  • Individuals who have received more than 4 CBT sessions for pain management in the past 6 months, as per their health-care provider and self-report

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

302 participants in 2 patient groups

iCanCope app and website
Experimental group
Description:
Intervention: Behavioral: iCanCope app and website
Treatment:
Behavioral: iCanCope app and website
Attention control group
Active Comparator group
Description:
Intervention: Behavioral: Attention control group
Treatment:
Behavioral: Attention control group

Trial contacts and locations

10

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Data sourced from clinicaltrials.gov

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