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Older people's exercise intervention in residential and nursing accommodation

Older People's Exercise intervention in Residential and nursing Accommodation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43769277
Enrollment
1000
Registered
2007-05-31
Start date
2008-02-01
Completion date
Unknown
Last updated
2018-02-26

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

Conditions

Depression Mental and Behavioural Disorders Depression

Interventions

All able residents of all participating homes will be invited to participate in a brief baseline assessment lasting 15-20 minutes, measuring cognitive function, mobility, pain and quality of life. We

Sponsors

Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Assessment: 1. Permanent resident in residential or nursing home 2. Aged 65 or over 3. Consent/assent to assessment 4. Able to participate in baseline assessment Record check: 5. Consent/assent Exercise classes: 6. Able to transfer (with assistance from one person) from a wheelchair to a chair

Exclusion criteria

Exclusion criteria: Terminal or other serious illness

Design outcomes

Primary

MeasureTime frame
Impact of the exercise intervention on depression levels measured through the use of the Geriatric Depression Scale (GDS) -15 at baseline and 12 months for all participants. For those who score highly on the GDS-15, we will also interview them at the 6-month stage in addition to the 2 timepoints for all residents.

Secondary

MeasureTime frame
1. Quality of life measured by EueroQoL 5 dimensions (EQ5D) at baseline and 12 months for all participants, and in addition at 6 months for those who score highly on the GDS-15. 2. Mobility measured by the Short Physical Performance Battery (SPPB) at baseline and 12 months for all participants, and in addition at 6 months for those who score highly on the GDS-15. 3. Injurious falls measured through home and hospital records. This will be collected at baseline, 3, 6, 9 and 12 months. 4. Cognitive function measured by the Mini Mental State Examination (MMSE) at baseline and 12 months for all participants, and in addition at 6 months for those who score highly on the GDS-15. 5. Pain, measured through participants' self reported level of pain on a five point scale at baseline and 12 months for all participants, and in addition at 6 months for those who score highly on the GDS-15. 6. Medication use, measured through their home records. This will be collected at baseline, 3, 6, 9 and 12 months. 7. Hospital Admissions. We will extract data on cause and duration of any hospital admissions during the study period from participants? hospital records.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 29, 2026