The Norwegian "iCanCope With Pain" App

Pain Clinical Trial

Official title:

Cultural Adaptation and Evaluation of the "iCanCope With Pain" App Among Norwegian Adolescents Living With Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03551977
• Other study ID #: 1310 63221
• Status: Completed
• Phase: N/A
• Start date: November 28, 2017
• Est. completion date: June 15, 2018

Study information

• Verified date: November 2022
• Source: University of Agder
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background: Research evidence shows that prevalence of pain in adolescents is increasing and is therefore recognized as a growing health problem. Psychological interventions delivered remotely through the internet may reduce intensity or severity of pain among children and adolescents with chronic pain. The iCanCope with Pain program is an existing web- and mobile-based self-management program, which is developed as a multi-center study funded by the Canadian Institutes of Health Research and is based on identified health care needs and current best practices for pain self-management. Objectives: The primary objectives are to describe the translation and cultural adaptation of the Norwegian version of the iCanCope with Pain mobile application and evaluate the effect in an upcoming randomized controlled trail with adolescents with chronic pain. Study sample: 16-19-year-old adolescents with self-declared persistent and/or chronic pain. Recruited from high schools in Southern Norway. Theoretical framework: Cognitive behavioral therapy (CBT) is explained by an integration of behavioral and cognitive theories of human behavior and psychopathology and is often the preferred treatment of choice for adolescents with different health disorders. The theoretical framework of CBT is integrated in the iCanCope with Pain app in terms of five components. The intervention group will receive the app with all five components: (I) symptom trackers for pain, sleep, mood, physical, and social function; (II) goal setting to improve pain and function; (III) coping toolbox of pain self-management strategies; (IV) social support; (V) age-appropriate pain education. The control group will receive the app with only the first self-registration component (I) symptom trackers for pain, sleep, mood, physical, and social function. Methods: Both qualitative and quantitative data will be gathered for evaluating the Norwegian version of the iCanCope with Pain app. Usability testing are assessed in both laboratory settings and in field using observation, interviews and questionnaires, which provide necessary information for an upcoming randomized controlled trail (RCT). Outcomes will in the RCT be measured at baseline (mid-April) and after an 8 weeks intervention (mid-June). The study is part of a PhD project.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 112
• Est. completion date: June 15, 2018
• Est. primary completion date: June 15, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 19 Years

Eligibility

Inclusion Criteria:

1. 16-19-year-old adolescents

2. with persistent and/or chronic pain, weekly suffered and lasting 3 months or more based on subjective reporting

3. be able to read and understand Norwegian

4. have their own smartphone.

Exclusion Criteria:

1. Adolescents with cognitive disability or diseases, because of the risk of not correctly understanding the iCanCope with Pain program via self-report, goal setting and/or library reading.

2. Adolescents that have participated in the usability testing of the Norwegian iCanCope with Pain app

3. Adolescents with diagnoses from a pathological or medical origin (e.g hematology/oncology patients) will also be excluded because the program was not specifically designed for these pain groups.

Related Conditions & MeSH terms

• Pain

Intervention

Behavioral:
• iCanCope with Pain
The participants are free to use the Norwegian iCanCope with Pain app as much as they want during the 8 week intervention period. The only support available is technical support.
• iCanCope with Pain control
The participants are free to use the Norwegian iCanCope with Pain control app as much as they want during the 8 week intervention period. The only support available is technical support.

Locations

Country	Name	City	State
Norway	Erik Grasaas	Kristiansand

Sponsors (2)

Lead Sponsor	Collaborator
University of Agder	The Hospital for Sick Children

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Attrition rate	Change in participants completed the post-questionnaire divided by the number of participants at baseline.	Baseline and 8-weeks
Primary	App engagement	Completion of daily symptom check-ins was used as a proxy for app engagement.	Baseline to 8 weeks.
Secondary	Physical activity	Change in total score of the International Physical Activity Questionnaire (IPAQ). Higher values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Coping	Change in total score of the General Self-Efficacy Questionnaire Short Version (GSEQ). Higher values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Social participation	Change in total score of school absence (General Information Questionnaire). Lower values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Over-The-Counter (OTC) analgesics	Change in total score of OTC analgesics consumption (General Information Questionnaire). Lower values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Perceived social support from friends	Change in total score of the Perceived Social Support from friends Questionnaire (PSS). Higher values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Pain self-efficacy questionnaire	Change in total score of the Pain Self-Efficacy Questionnaire (PSEQ). Higher values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Anxiety and depression	Change in total score of the Hospital Anxiety and Depression Scale Questionnaire (HADS). Lower values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Global impression of change	Change in Patients' Global Impression of Change Scale (PGIC) from 1-7. Higher values at post-intervention represent a better outcome.	After 8 weeks (post-intervention)
Secondary	Health-related quality of life (HRQOL)	Change in total score of the Kidscreen 52 Questionnaire. Higher values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)
Secondary	Pain experience	Change in total score of the Lubeck Pain Questionnaire (LPQ). Lower values at post-intervention represent a better outcome.	Baseline and 8 weeks (post-intervention)