Effectiveness of self-management programs among athletes with patellofemoral pain syndrome : protocol for a systematic review

dc.contributor.authorMasoudi, Ameen
dc.contributor.authorChemane, Nomzamo
dc.contributor.authorUseh, Ushotanefe
dc.contributor.authorBello, Bashir
dc.contributor.authorMagida, Nontembiso
dc.date.accessioned2024-11-29T12:14:43Z
dc.date.available2024-11-29T12:14:43Z
dc.date.issued2024-11
dc.descriptionDATA AVAILABILITY : All data will be available via contacting the corresponding author upon request.en_US
dc.description.abstractBACKGROUND : Patellofemoral pain syndrome is a highly prevalent overuse knee injury in athletic populations associated with pain and functional limitations, exacerbated by activities such as running, pivoting, cycling, and jumping. Self-management programs empowering athletes to take an active role in controlling their symptoms for chronic musculoskeletal conditions such as patellofemoral pain syndrome have grown in popularity. However, the efficacy of self-management programs specifically for athletes with patellofemoral pain syndrome is unclear due to limited and heterogeneous evidence. OBJECTIVE : The systematic review study will evaluate the effectiveness of self-management programs on pain and function, in athletes with patellofemoral pain syndrome. METHODS : PubMed/MEDLINE, Cochrane Library, CINAHL (Cumulative Index to Nursing and Allied Health Literature), and PsycINFO databases will be systematically searched using terms related to “patellofemoral pain syndrome,” “self-management,” and “athletes.” Interventional studies that are randomized and nonrandomized controlled trials will be included, comparing self-management programs to other treatments or control conditions among athletes with patellofemoral pain syndrome. Four reviewers will independently screen studies, extract data using the COVIDENCE software, and assess the quality of the study and evidence using the Pedro scale of risk of bias tool and GRADE approach, respectively. If feasible, a meta-analysis will be performed using the RevMan (version 5.4; the Cochrane Collaboration). RESULTS : The systematic review is currently in the search phase, with the authors refining search strings for the selected databases. The final search strings are expected to be ready by March 2024, and the review is projected to be completed by July 2024. CONCLUSIONS : This systematic review protocol outlines a rigorous methodology for evaluating the effectiveness of self-management programs among athletes with patellofemoral pain syndrome. The findings will inform clinical practice and guide the development of tailored interventions to optimize outcomes for athletes with patellofemoral pain syndrome. TRIAL REGISTRATION : PROSPERO CRD42023492746; https://tinyurl.com/c5jze9ca INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID) : PRR1-10.2196/58340en_US
dc.description.departmentPhysiotherapyen_US
dc.description.librarianhj2024en_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.urihttps://www.researchprotocols.org/en_US
dc.identifier.citationMasoudi, A., Chemane, N., Useh, U. et al. 2024, 'Effectiveness of self-management programs among athletes with patellofemoral pain syndrome : protocol for a systematic review', JMIR Research Protocols, vol. 13, art. e58340, pp. 1-6, doi : 10.2196/58340.en_US
dc.identifier.issn1929-0748 (online)
dc.identifier.other10.2196/5834
dc.identifier.urihttp://hdl.handle.net/2263/99696
dc.language.isoenen_US
dc.publisherJMIR Publicationsen_US
dc.rights© Ameen Masoudi, Nomzamo Chemane, Ushotanefe Useh, Bashir Bello, Nontembiso Magida. This is an open-access article distributed under the terms of the Creative Commons Attribution License.en_US
dc.subjectPatellofemoral pain syndrome (PFPS)en_US
dc.subjectAthletesen_US
dc.subjectSelf-managementen_US
dc.subjectChronic painen_US
dc.subjectPain managementen_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.titleEffectiveness of self-management programs among athletes with patellofemoral pain syndrome : protocol for a systematic reviewen_US
dc.typeArticleen_US

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