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Occupational Therapy for Cancer Patients: a Randomised, Controlled Study

Occupational Therapy for Cancer Patients: A Randomised Controlled Study

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01432197
Enrollment
116
Registered
2011-09-12
Start date
2010-03-31
Completion date
Unknown
Last updated
2011-09-12

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

Conditions

HRQOL (Health Related Quality of Life)

Keywords

HRQOL, Occupational therapy, ADL intervention, Cancer patients

Brief summary

The aim of this study is to investigate the effect of occupational therapy, in shape of activities of daily living, for cancer patients.

Detailed description

Background Cancer patients often experience serious dysfunctions leading to problems with activities of daily living (ADL) and reduced quality of life. Occupational therapy is believed to be effective in handling many of the problems with ADL experienced by patients with cancer, but the evidence is sparse. Aim The purpose of this study is to analyse the effects of an occupational therapy intervention targeting cancer patients. Outcome measures are the patients self-reported quality of life and the patients ability to perform ADL. Methods Randomised controlled trial with 288 patients with cancer treated at Naestved hospital in Denmark. Occupational therapy intervention programme for the intervention group (N=144) and standard treatment and care for the controls (N=144). A systematic review including studies of ADL intervention for cancer patients will be carried out. Feasibility of the recruitment and the intervention will be analysed and published. The patients need for occupational therapy will be analysed using baseline information from the randomised controlled trial. The effects of the intervention will be analysed using patient validated questionnaires including EORTC QLQ-C30 and the ADL taxonomy questionnaire.

Interventions

1\) ADL training, 2) home modifications, 3) delivery and supervision in adaptive equipments, and 4) instruction in self-training programs.

Sponsors

Naestved Hospital
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Cancer patients * Disability comparable with a performance status of 10 to 70 on Karnofsky Performance Status Scale * Able to read and understand Danish

Exclusion criteria

* Referred to occupational therapy before study start

Design outcomes

Primary

MeasureTime frame
Health related quality of life15 months

Secondary

MeasureTime frame
Ability to perform activities of daily living15 months

Countries

Denmark

Outcome results

None listed

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