Skip to content

The Social Fitness Study

What is the effectiveness of a tailor-made social fitness program for community dwelling older people with dementia and their caregivers?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24186
Enrollment
92
Registered
2013-12-23
Start date
2014-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

dementia, memory problems, caregivers, social participation, psychosocial intervention, occupational therapy, physiotherapy, welfare/ dementie, geheugenproblemen, mantelzorgers, sociale participatie, psychosociale interventies, ergotherapie, fysiotherapie, welzijnswerk.

Interventions

In the experimental group, patients and their caregivers will receive treatment and guidance according to the newly develloped Social Fitness Programme (SFP). SFP contains up to two interdisciplinary

Sponsors

Radboud university medical center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Eligible participants for this study meet all of the following criteria: - Home dwelling patients with dementia diagnosis (MMSE ≥10); or home dwelling patients with memory problems signaled by the referring professional (MMSE 10-24); or home dwelling patients with memory problems and with high intelligence or high levels of education resulting in an MMSE-score between 25 and 30, with a primary caregivers’ score of ≥3.6 on the IQCODE-N. - Who have a caregiver who is available for informal support at a minimum of one time a week. - The patient and caregiver wish to maintain or improve their level of social participation, or to decrease their feelings of loneliness.

Exclusion criteria

Exclusion criteria: 1. No goals in total (patient and caregiver together) for social participation. 2. People who are not capable of completing the self assessment forms. 3. Co-morbidity with symptoms that interfere with actively taking part in the intervention 4. Not stable use (< 3 months on the same dose) of medication which influences cognition 5. Palliative phase of illness 6. Acute illness with hospital indication 7. Current participation in other health research 8. Received physiotherapy according to the Coach2Move protocol in the last 6 months. 9. Received occupational therapy according to the COTiD-programme in the last 6 months. 10. No financial possibilities to receive occupational therapy

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is patients' and caregivers' participation in meaningful social activities, assessed with the performance and satisfaction rating of the Canadian Occupational Performance Measurement (COPM).

Secondary

MeasureTime frame
Patients' and caregivers' quality of life (DQoL) and health related quality of life (EQ-5D); patients’ mobility (TUG), caregivers’ sense of competence (SCQ); resource utilization (RUD 4.0) and socio-demographics. Patients' frailty is measured as a covariate (EFIP).

Contacts

Public ContactHanneke Donkers

Radboud UMC

Hanneke.Donkers@radboudumc.nl-

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)