Study and Analysis of Biomechanical Parameters of Human Movement Based on Disability Indicators in Older Adults

NCT05611723 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2024-11-07

No results posted yet for this study

Summary

Older adults develop modifications in the execution of movement that lead to impairments in activities of daily living performance. Accordingly, there is a need for technological advances in devices that assist older adults targeting improvements in parameters of movement performance that have the highest impact on the skills of daily living. Therefore, to gather the parameters of movement impacting daily living activities, the main goal of this study is to perform a comparative analysis of the biomechanical movement parameters between older adults with and without disability, performing the tasks: gait, sit-to-stand, timed up and go, quiet standing and climb and descend stairs.

This work was supported by theFundação para a Ciência e Tecnologia (FCT), \[grant number 2020.05356.BD\] and through R\&D Units funding \[UIDB/05210/2020\], Fundação para a Ciência e Tecnologia (FCT), Portugal and the European Union.

Conditions

  • Disability

Interventions

OTHER

Exposure to disability

Disability status assessed by functional measures

Sponsors & Collaborators

  • Center for Rehabilitation Research - Polytechnic Institute of Porto (IPP)

    collaborator UNKNOWN
  • Universidade do Porto

    collaborator OTHER
  • School of Allied Health Sciences of Porto (ESTSP) - Polytechnic Institute of Porto (IPP)

    collaborator OTHER
  • Polytechnic Institute of Porto

    lead OTHER

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-01
Primary Completion
2023-04-30
Completion
2024-11-02

Countries

  • Portugal

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05611723 on ClinicalTrials.gov