Objective To assess the ability to generate both kinesthetic and visual motor imagery in participants with chronic shoulder pain, compared with asymptomatic subjects. To assess the influence of psychosocial and motor variables in the motor imagery process.
Methods A cross-sectional observational study was conducted with a non-probability sample of 30 participants, divided into 15 patients with chronic shoulder pain and 15 asymptomatic subjects. Participants completed socio-demographic questionnaires, followed by assessment of mental imagery and mental chronometry using the MIQ-R questionnaire, as well as range of motion and grip strength.
Results Our results indicated that patients with chronic shoulder pain had difficulty generating kinesthetic and visual MI (p<0.05; d>0.80) and also took a longer time to imagine them (p<0.05; d>-0.80). A moderate-positive association was found between the levels of CPSS and the kinesthetic motor imagery ability (r=0.54, p=0.035), explaining 24.5% of the variance. In addition, a moderate-positive association was also found between the strength of the affected upper limb with the total score of MIQ-R (r=0.56, p=0.037), explaining 25.7% of the variance.
Conclusions Based on the obtained results, it seems that patients with chronic shoulder pain have greater difficulty with generating both kinesthetic and visual motor images compared to asymptomatic subjects, and they also needed more time to perform the mental tasks. It was found that psychosocial state and motor condition may influence the imagining ability of patients with chronic shoulder pain. Further research is needed to improve our understanding and to be able to establish clinical implications.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
This study was approved by the ethics committee of University La Salle (CSEULS- PI-031/2022).
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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