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The investigation of the effects of occupational therapy's intervention on occupational performance in advanced cancer patients

The Investigation of the effects of Occupational Therapy's Interventions on Occupational Performance in advanced cancer patients at home during covid-19 crisis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180908040970N2
Enrollment
70
Registered
2021-11-29
Start date
2021-11-21
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Advanced Cancer. Encounter for palliative care

Interventions

Intervention 1: Control group: Receive home-care services and traditional palliative care. Since occupational therapy services are not currently available to cancer patients, if the patient is referre

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: patients with advanced cancer age range of 18 to 65 years old having an acceptable level of cognitive function as a score of 21 or higher based on the Mini Mental Status Examination (MMSE) In at least one case the Katz questionnaire needs help

Exclusion criteria

Exclusion criteria: Existence of other diseases such as neurological problems, orthopedics and mental disorders.

Design outcomes

Primary

MeasureTime frame
Occupational Performance rate in the Canadian Occupational Performance Measure. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: Canadian Occupational Performance Measure(COPM).;Level of Quality Of Life. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: European Organization for Research and Treatment of Cancer-of-life Questionnaire Core30 (EORTC QLQ-30 ).;Ability to perform Activities of Daily Living. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: Katz Index.

Secondary

MeasureTime frame
Ability to perform Instrumental Activities of Daily Living. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: The Lawton Instrumental Activity of Daily Living.;The amount of pain. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: Brief Pain Inventory.;The amount of fatigue. Timepoint: Time intervals for evaluation at the beginning of the study(before the interventions), and by passing 6nd, and 14th weeks from the intervention(Follow-up). Method of measurement: Cancer Fatigue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Raissi

Iran University of Medical Sciences

graissi@gmail.com+98 21 8214 1612

Outcome results

None listed

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