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dc.contributor.authorMajor, Daniel Høgli
dc.contributor.authorGrotle, Margreth
dc.contributor.authorLittlewood, Chris
dc.contributor.authorBrox, Jens Ivar
dc.contributor.authorMatre, Dagfinn
dc.contributor.authorGallet, Heidi V.
dc.contributor.authorRøe, Yngve
dc.date.accessioned2021-02-08T14:42:39Z
dc.date.accessioned2021-03-11T14:36:23Z
dc.date.available2021-02-08T14:42:39Z
dc.date.available2021-03-11T14:36:23Z
dc.date.issued2021-01-25
dc.identifier.citationMajor DH, Grotle M, Littlewood C, Brox JI, Matre D, Gallet, Røe Y. Adherence to self-managed exercises for patients with persistent subacromial pain. The Ad-Shoulder feasibility study. BMC Pilot and Feasibility Studies. 2021;7en
dc.identifier.issn2055-5784
dc.identifier.urihttps://hdl.handle.net/10642/10014
dc.description.abstractBackground: Exercise is recommended for patients with subacromial pain. It has been suggested that good exercise adherence improves clinical outcomes. Despite this, little attention has been paid to the need for behavioural frameworks to enhance adherence to home exercise programmes for patients with subacromial pain. Methods: A feasibility study with pre-post design was used. Participants aged > 18 years, with subacromial pain, who had received conservative treatment during the past 6 months, were recruited. The Ad-Shoulder intervention consisted of 1–5 individual sessions provided over 3 months and was based on 5 self-management skills, which aimed to enhance the patients’ self-efficacy and adherence to self-managed exercises. The primary objectives were assessed according to predefined progression criteria: (1) the recruitment rate (10 patients enrolled within 12 weeks), (2) follow-up rate (≥ 80% on all self-reported measures), (3) objective physical activity measures (≥ 80% of participants would contribute valid data at each time point), (4) adherence with the self-managed exercises (≥ 80% of the participants would adhere to ≥ 80% of the assigned home exercise programme), (5) fidelity of the delivery of the intervention (the therapists delivered the intervention according to the protocol) and (6) adverse events (< 30% would report adverse events (including mild)). The results were reported using descriptive statistics. Results: Eleven patients were recruited during 16 weeks. Ten patients completed the self-reported measures at baseline and week 12. Objective physical activity measures were successfully obtained for 100% (11/11) at baseline, 64% (7/11) at week six and 82% at week 12. Fifty-five percent (6/11) of the participants satisfactorily completed at least 80% of their home exercise programme. All sessions were delivered according to the protocol. None of the patients reported any adverse events. Conclusions: Objective physical activity data measures at baseline and week 12, follow-up, the physiotherapists’ fidelity to the intervention and adverse events met our pre-specified progression criteria. Recruitment and adherence to the self-managed exercise programme were both below the anticipated level. Further intervention development is necessary to understand whether adherence to the self-managed exercises could be enhanced and additional methods of recruitment would need to be considered, including additional recruitment sites, in any planning for a future main trial.en
dc.language.isoenen
dc.publisherBMCen
dc.relation.ispartofseriesPilot and Feasibility Studies;7, Article number: 31 (2021)
dc.rightsCreative Commons Attribution 4.0 International (CC BY 4.0) Licenseen
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectSelf-managed exercisesen
dc.subjectPatientsen
dc.subjectPersistent subacromial painsen
dc.subjectFeasibility studiesen
dc.subjectPhysical data
dc.subjectExercise programmes
dc.titleAdherence to self-managed exercises for patients with persistent subacromial pain. The Ad-Shoulder feasibility studyen
dc.typeJournal articleen
dc.typePeer revieweden
dc.date.updated2021-02-08T14:42:39Z
dc.description.versionpublishedVersionen
dc.identifier.doihttps://doi.org/10.1186/s40814-021-00767-6
dc.identifier.cristin1878159
dc.source.journalBMC Pilot and Feasibility Studies


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