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Effect of occupational therapy in elderly people living at home

Effect of a home-based occupational therapy rehabilitation program ? A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93873801
Enrollment
100
Registered
2013-05-24
Start date
2012-09-01
Completion date
Unknown
Last updated
2019-02-11

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

Conditions

Occupational therapy for elderly citizens Not Applicable

Interventions

1. Intervention: Occupational therapy 2. Control: Treatment as usual Citizens randomised to the intervention group will receive 60 minutes training by an occupational

Sponsors

VIA University College (Denmark)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Citizens from 60 years of age, either sex 2. Living at home or in sheltered housing 3. Admissioned to either personal help and/or practical help and meal delivery from the municipality

Exclusion criteria

Exclusion criteria: 1. Citizens living in assisted living facilities 2. Having a serious mental illness, dementia, mentally handicapped 3. Suffering from cancer or severe pain

Design outcomes

Primary

MeasureTime frame
Changes in self-reported occupational performance (COPM score) are calculated for the intervention and control groups and tested by Wilcoxon Rang Sum Test in order to statistically test if any difference between the two groups occur. Measured at 0 (baseline), 3, and 6 months.

Secondary

MeasureTime frame
1. Changes in satisfaction with own occupational performance (COPM score) are calculated for the intervention and control groups and tested by the Wilcoxon Rang Sum Test in order to statistically test if any any differences between the two groups occur. 2. Changes in motor and process skills (AMPS score) are calculated for the intervention and control groups and tested by a Wicoxon Rang Sum Test in order to test if any statistically significant difference occur between the two groups. 3. Changes in Quality of life (SF-36) are calculated for the intervention and control groups and between groups differences will be tested by T-test if data are normally distributed, or by a Wilcoxon Rang Sum Test if they are not normally distributed. Measured at 0 (baseline), 3, and 6 months.

Countries

Denmark

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026