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Clinical Trials/NCT03505385
NCT03505385
Completed
Not Applicable

Effects of a Unique Co-created Intervention With Care Home Residents and University Students Following a Service-learning Methodology to Reduce Sedentary Behaviour.

Glasgow Caledonian University1 site in 1 country33 target enrollmentMay 20, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physical Activity
Sponsor
Glasgow Caledonian University
Enrollment
33
Locations
1
Primary Endpoint
Change in sitting time
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Background. There is a growing demand for long-term care settings. Care-home residents are a vulnerable group with high levels of physical dependency and cognitive impairment. Long-term care facilities' policy need to adapt and offer more effective and sustainable interventions to address their complex physical and mental health needs. Despite the increasing emphasis on patient and public involvement, marginalised groups such as care-home residents, can be overlooked when including people in the research process. The GET READY project aims to integrate service-learning methodology into Physical Therapy and Sport Sciences University degrees by offering students individual service opportunities (placements) with residential care homes, in order to co-create the best suited intervention with researchers, older adults of both genders (end-users) in care homes, health professionals, caregivers, family members and policy makers.

Methods. Stage 1 will integrate a service-learning methodology within a Physical Therapy module in Glasgow and Sport Sciences module in Barcelona, design two workshops for care home residents and conduct a co-creation protocol. Stage 2 will assess the intervention feasibility, safety and preliminary effects of the co-created intervention in a group of 33 care home residents, within a two-armed pragmatic randomized clinical trial.

Registry
clinicaltrials.gov
Start Date
May 20, 2019
End Date
January 15, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Care Home residents ≥ 70 years old.

Exclusion Criteria

  • Comorbidity preventing participation (e.g. severe breathlessness, pain, or severe neurological disease).
  • Life expectancy of less than one year.
  • Being unlikely to undertake the intervention regularly.
  • Severe dementia.

Outcomes

Primary Outcomes

Change in sitting time

Time Frame: During 7 days. Outcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks).

Number of minutes spent in a sitting position with ActivPal monitor.

Change in minutes spent in sedentary behaviour

Time Frame: During 7 days. Outcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks)

Number of minutes spent in activities requiring ≤ Metabolic Equivalent Tasks with ActivPal monitor.

Secondary Outcomes

  • Physical Function(Outcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks).)
  • Change in health-related quality of life(Outcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks).)

Study Sites (1)

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