Effect of neck-specific exercises with and without internet support on cervical range of motion and neck muscle endurance in chronic whiplash-associated disorders: analysis of functional outcomes of a randomized controlled trialShow others and affiliations
2024 (English)In: Journal of Rehabilitation Medicine, ISSN 1650-1977, E-ISSN 1651-2081, Vol. 56, article id 34785Article in journal (Refereed) Published
Abstract [en]
OBJECTIVE: To compare the effects of a neck-specific exercise programme with internet support and 4 physiotherapist sessions (NSEIT) and the same neck-specific exercises supervised by a physiotherapist (NSE) on neck muscle endurance and cervical range of motion. DESIGN: Randomized controlled trial. PATIENTS: A total of 140 participants with chronic whiplash-associated disorders grade II or grade III were randomly assigned to the NSEIT or NSE groups.
METHODS: Outcomes were changes in active cervical range of motion, cranio-cervical flexion test, neck muscle endurance, and neck pain, at 3- and 15-month follow-ups.
RESULTS: There were no significant differences between the NSEIT and NSE groups. There was a significant group-by-time inter-action effect in active cervical range of motion flexion/extension where the NSEIT group improved to 3-month follow-up, but the NSE group did not. Both groups were significantly improved over time in all other outcomes (p < 0.001) at 3- and 15-month follow-ups, with effect size between 0.64 and 1.35 in active cervical range of motion, cranio-cervical flexion test, dorsal neck muscle endurance, and neck pain, and effect size between 0.22 and 0.42 in ventral neck muscle endurance.
CONCLUSION: Both NSE and NSEIT led to improved neck function. Depending on the patients' needs, either NSE or NSEIT could be used as treatment for patients with chronic whiplash-associated disorders.
Place, publisher, year, edition, pages
Foundation for Rehabilitation Information , 2024. Vol. 56, article id 34785
National Category
Physiotherapy
Identifiers
URN: urn:nbn:se:oru:diva-115426DOI: 10.2340/jrm.v56.34785ISI: 001280772600001PubMedID: 39072427Scopus ID: 2-s2.0-85201597084OAI: oai:DiVA.org:oru-115426DiVA, id: diva2:1889769
Funder
Vinnova, 2018-02244Swedish Research Council, 2018-02476Uppsala University, 736751; 854531; 930399Södra sjukvårdsregionen, 844451; 939838Region Östergötland, 676261; 847691
Note
The study was funded by: Vinnova (grant number 2018-02244), the Swedish Research Council (grant number 2018-02476), the Centre for Clinical Research Sörmland at Uppsala University Sweden (grant numbers 736751, 854531, 930399), the Regional Research Council Mid Sweden (grant number 641551, 838701, 939243), the Medical Research Council of Southeast Sweden (grant numbers 844451, 939838), and Östergötland County Council (grant numbers 676261, 847691).
2024-08-162024-08-162025-02-11Bibliographically approved