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dc.contributor.authorMena-Del Horno, Silvia
dc.contributor.authorDueñas, Lirios
dc.contributor.authorLluch, Enrique
dc.contributor.authorLouw, Adriaan
dc.contributor.authorLuque-Suarez, Alejandro
dc.contributor.authorMertens, Michel Gcam
dc.contributor.authorFuentes-Aparicio, Laura
dc.contributor.authorBalasch-Bernat, Mercè
dc.date.accessioned2024-02-27T15:15:50Z
dc.date.available2024-02-27T15:15:50Z
dc.date.issued2022-02-24
dc.identifier.otherhttp://hdl.handle.net/10668/21035
dc.identifier.urihttp://hdl.handle.net/20.500.12105/18765
dc.description.abstractBackground: Frozen shoulder (FS) is a highly disabling pathology of poorly understood etiology, which is characterized by the presence of intense pain and progressive loss of range of motion (ROM). The aim of this study is to evaluate the feasibility and clinical impact of a CNS-focused treatment program for people with FS. Methods: 10 subjects with primary FS received a 10-week CNS-focused intervention including sensory discrimination training and graded motor imagery techniques delivered as clinic sessions (60 min) and home therapy (30 min five times per week). Measurements were taken at baseline, after a 2-week “washout” period, after treatment, and at three months follow-up. The Shoulder Pain and Disability Index (SPADI) was the primary outcome. Secondary measures were feasibility-related outcomes, self-reported shoulder pain, active and passive range of motion, two-point discrimination threshold (TPDT), left/right judgement task (LRJT), fear-avoidance (Tampa Scale for Kinesiophobia), pain catastrophization (Pain Catastrophizing Scale), and pain sensitization (Central Sensitization Inventory). A Student’s t-test was used to assess the “washout” period. A repeated measure analysis of variance (ANOVA) was used to evaluate within-subjects’ differences for all outcome measures in the different assessment periods and a pairwise analysis was used to compare between the different assessment points. Statistical significance was set at p < 0.05. Results: 70% of participants completed the treatment. No significant changes were found after “washout” period except for TPDT (p = 0.02) and SPADI (p = 0.025). Improvements in self-reported shoulder pain (p = 0.028) and active shoulder flexion (p = 0.016) were shown after treatment (p = 0.028) and follow-up (p = 0.001) and in SPADI at follow-up (p = 0.008). No significant changes were observed in TPDT, LRJT, fear-avoidance, pain catastrophization, and pain sensitization. Conclusions: a CNS-focused treatment program might be a suitable approach to improve pain and disability in FS, but further research is needed to draw firm conclusions.
dc.language.isoeng
dc.type.hasVersionVoR
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectadhesive capsulitis
dc.subjectfeasibility study
dc.subjectfrozen shoulder
dc.subjectmotor imagery
dc.subjectpatient compliance
dc.subjecttactile discrimination training
dc.subject.meshBursitis 
dc.subject.meshCentral Nervous System 
dc.subject.meshFeasibility Studies 
dc.subject.meshHumans 
dc.subject.meshRange of Motion, Articular
dc.subject.meshShoulder Pain 
dc.subject.meshTreatment Outcome 
dc.titleA Central Nervous System Focused Treatment Program for People with Frozen Shoulder: A Feasibility Study.
dc.typeresearch article
dc.rights.licenseAttribution 4.0 International*
dc.identifier.pubmedID35270316es_ES
dc.format.volume19es_ES
dc.format.number5es_ES
dc.identifier.doi10.3390/ijerph19052628
dc.identifier.e-issn1660-4601es_ES
dc.identifier.journalInternational journal of environmental research and public healthes_ES
dc.rights.accessRightsopen accesses_ES


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Attribution 4.0 International
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