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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03505385
Acronym
GET READY
Enrollment
33
Registered
2018-04-23
Start date
2019-05-20
Completion date
2020-01-15
Last updated
2020-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Care Home Residents, Physical Activity, Sedentary Behaviour

Keywords

Co-creation, Service-learning methodology

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.

Interventions

BEHAVIORALCo-created intervention - Get Ready (GR)

The Get Ready (GR) intervention was delivered one-to-one with the care home resident and a relevant family member during a 12-week period: 1. The familiarisation stage aimed to build a rapport with two long-term achievement goals to sit less and move more with the resident and the family member and consisted of two sessions, one in week 1 (50-60minutes) and the other in week 3 (30-40 minutes). 2. The ramping up stage aimed to review the rapport and reach an achievable consensus with the resident and the family member. It consisted of two sessions, one in week 5 and the other in week 7 (20-30 minutes each). 3. The maintenance stage aimed at integrating behaviours and included two sessions, one in week 9 and the other at week 12 (20-30 minutes each). Sessions 5 and 6 were used to understand how the resident was getting on with their short-term GR goals, facilitating some problem-solving discussions.

Sponsors

Glasgow Caledonian University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in minutes spent in sedentary behaviourDuring 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.
Change in sitting timeDuring 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.

Secondary

MeasureTime frameDescription
Change in health-related quality of lifeOutcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks).EuroQoL - 5D
Physical FunctionOutcome measure will be collected at baseline and at the end of the intervention (up to 24 weeks).Short Physical Performance Battery

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026