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Randomised Controlled Trial of Unsolicited Occupational Therapy in Community-Dwelling Elderly

Randomised Controlled Trial of Unsolicited Occupational Therapy in Community-Dwelling Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00278096
Enrollment
400
Registered
2006-01-18
Start date
2000-03-31
Completion date
2004-05-31
Last updated
2006-01-18

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

Conditions

Disability, Occupational Therapy

Keywords

disability, occupational therapy

Brief summary

In this study we aim to assess whether unsolicited occupational therapy compared to no therapy can decelerate the increase in disability in high-risk elderly.

Detailed description

Community-dwelling elderly, and particularly the oldest old, are generally viewed as highly susceptible to the 'inverse care law'. That is, those in greatest need for preventive assessment and surveillance have the highest potential benefit but are most likely to be missed. Hence, active case-finding and close follow-up might be an important strategy for maintaining the health, independence, and well-being of very elderly people who are at a particularly high risk. In this study we aim to assess whether unsolicited occupational therapy compared to no therapy can decelerate the increase in disability in high-risk elderly. Subjects in the intervention group will be visited by an occupational therapist who provides training and education about assistive devices that are already present and will give recommendations and information about procedures, possibilities, and costs of assistive devices and community-based services. Control subjects will not be visited by an occupational therapist. The primary outcome measure of the trial will be the score on the Groningen Activity Restriction Scale (GARS). Secondary outcome measures will be well-being and feelings of loneliness.

Interventions

BEHAVIORALoccupational therapy

Sponsors

Netherlands Organisation for Scientific Research
CollaboratorOTHER_GOV
Leiden University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
85 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* age 85 years * living independently * MMSE score \> 18 points

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
Score on the Groningen Activity Restriction Scale (GARS)

Secondary

MeasureTime frame
Well-being and feelings of loneliness.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026