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dc.contributor.authorGrasaas, Erik
dc.contributor.authorHelseth, Sølvi
dc.contributor.authorFegran, Liv
dc.contributor.authorStinson, Jennifer
dc.contributor.authorSmåstuen, Milada Cvancarova
dc.contributor.authorLalloo, Chitra
dc.contributor.authorHaraldstad, Kristin
dc.date.accessioned2022-11-15T13:10:45Z
dc.date.available2022-11-15T13:10:45Z
dc.date.created2022-10-13T13:29:38Z
dc.date.issued2022
dc.identifier.citationGrasaas, E., Helseth, S., Fegran, L., Stinson, J., Småstuen, M., Lalloo, C. & Haraldstad, K. (2022). App-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trial. BMC Pilot and Feasibility Studies, 8, 1-10.en_US
dc.identifier.issn2055-5784
dc.identifier.urihttps://hdl.handle.net/11250/3031935
dc.description.abstractBackground: Persistent pain in adolescence adversely afects 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 diferences 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 PainTM 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-efcacy, pain self-efcacy, 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 difer between the 2 groups. No diferences 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 signifcant diferences in outcomes between groups. However, the large efect 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 fullscale randomized controlled trial to improve participant retention.en_US
dc.language.isoengen_US
dc.publisherBioMed Central (BMC)en_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleApp-based intervention among adolescents with persistent pain: a pilot feasibility randomized controlled trialen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2022 The Author(s)en_US
dc.subject.nsiVDP::Medisinske Fag: 700::Helsefag: 800en_US
dc.source.pagenumber1-10en_US
dc.source.volume8en_US
dc.source.journalBMC Pilot and Feasibility Studiesen_US
dc.identifier.doihttps://doi.org/10.1186/s40814-022-01113-0
dc.identifier.cristin2061163
dc.source.articlenumber158en_US
cristin.qualitycode1


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