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App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial

BACKGROUND: Persistent pain in adolescence adversely affects everyday life and is an important public health problem. The primary aim was to determine the feasibility of an 8-week app-based self-management intervention to reduce pain and improve health-related quality of life in a community-based po...

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Autores principales: Grasaas, Erik, Helseth, Sølvi, Fegran, Liv, Stinson, Jennifer, Småstuen, Milada, Lalloo, Chitra, Haraldstad, Kristin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327289/
https://www.ncbi.nlm.nih.gov/pubmed/35897086
http://dx.doi.org/10.1186/s40814-022-01113-0
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author Grasaas, Erik
Helseth, Sølvi
Fegran, Liv
Stinson, Jennifer
Småstuen, Milada
Lalloo, Chitra
Haraldstad, Kristin
author_facet Grasaas, Erik
Helseth, Sølvi
Fegran, Liv
Stinson, Jennifer
Småstuen, Milada
Lalloo, Chitra
Haraldstad, Kristin
author_sort Grasaas, Erik
collection PubMed
description BACKGROUND: Persistent pain in adolescence adversely affects everyday life and is an important public health problem. The primary aim was to determine the feasibility of an 8-week app-based self-management intervention to reduce pain and improve health-related quality of life in a community-based population of adolescents with persistent pain. A secondary aim was to explore differences in health outcomes between the intervention and control groups. METHODS: A sample of 73 adolescents aged 16–19 years with persistent pain from a community-based population were randomized into 2 groups. The intervention group received the Norwegian culturally adapted version of the iCanCope with Pain(TM) app, which includes symptom tracking, goal setting, self-management strategies, and social support. The attention control group received a symptom tracking app. Feasibility was assessed as attrition rates and level of engagement (interactions with the app). The secondary outcomes included pain intensity, health-related quality of life, self-efficacy, pain self-efficacy, perceived social support from friends, anxiety and depression, and patient global impression. Statistical analyses were conducted using SPSS. RESULTS: Demographic and baseline outcome variables did not differ between the 2 groups. No differences were found between the participants completing the study and those who withdrew. Twenty-eight adolescents completed the intervention as planned (62% attrition). Both groups had a low level of app engagement. Intention-to-treat analysis (n = 19 + 14) showed no significant differences in outcomes between groups. However, the large effect size (Cohen’s d = .9) for depression suggested a lower depression score in the intervention group. CONCLUSIONS: High treatment attrition and low engagement indicate the need for changes in trial design in a full-scale randomized controlled trial to improve participant retention. TRIAL REGISTRATION: The iCanCope with Pain Norway trial was retrospectively registered in Clinical Trials.gov (ID: NCT03551977). Registered 6 June 2018. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40814-022-01113-0.
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spelling pubmed-93272892022-07-28 App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial Grasaas, Erik Helseth, Sølvi Fegran, Liv Stinson, Jennifer Småstuen, Milada Lalloo, Chitra Haraldstad, Kristin Pilot Feasibility Stud Research BACKGROUND: Persistent pain in adolescence adversely affects everyday life and is an important public health problem. The primary aim was to determine the feasibility of an 8-week app-based self-management intervention to reduce pain and improve health-related quality of life in a community-based population of adolescents with persistent pain. A secondary aim was to explore differences in health outcomes between the intervention and control groups. METHODS: A sample of 73 adolescents aged 16–19 years with persistent pain from a community-based population were randomized into 2 groups. The intervention group received the Norwegian culturally adapted version of the iCanCope with Pain(TM) app, which includes symptom tracking, goal setting, self-management strategies, and social support. The attention control group received a symptom tracking app. Feasibility was assessed as attrition rates and level of engagement (interactions with the app). The secondary outcomes included pain intensity, health-related quality of life, self-efficacy, pain self-efficacy, perceived social support from friends, anxiety and depression, and patient global impression. Statistical analyses were conducted using SPSS. RESULTS: Demographic and baseline outcome variables did not differ between the 2 groups. No differences were found between the participants completing the study and those who withdrew. Twenty-eight adolescents completed the intervention as planned (62% attrition). Both groups had a low level of app engagement. Intention-to-treat analysis (n = 19 + 14) showed no significant differences in outcomes between groups. However, the large effect size (Cohen’s d = .9) for depression suggested a lower depression score in the intervention group. CONCLUSIONS: High treatment attrition and low engagement indicate the need for changes in trial design in a full-scale randomized controlled trial to improve participant retention. TRIAL REGISTRATION: The iCanCope with Pain Norway trial was retrospectively registered in Clinical Trials.gov (ID: NCT03551977). Registered 6 June 2018. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40814-022-01113-0. BioMed Central 2022-07-27 /pmc/articles/PMC9327289/ /pubmed/35897086 http://dx.doi.org/10.1186/s40814-022-01113-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Grasaas, Erik
Helseth, Sølvi
Fegran, Liv
Stinson, Jennifer
Småstuen, Milada
Lalloo, Chitra
Haraldstad, Kristin
App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title_full App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title_fullStr App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title_full_unstemmed App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title_short App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
title_sort app-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327289/
https://www.ncbi.nlm.nih.gov/pubmed/35897086
http://dx.doi.org/10.1186/s40814-022-01113-0
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