Occupational Therapy in Palliative Care

January 8, 2020 updated by: M.D. Anderson Cancer Center

Is Inpatient Occupational Therapy Perceived to be Beneficial by the Palliative Patient and Caregiver?

The goal of this research study is to learn if inpatient occupational therapy can help patients in the Palliative Care Unit (PCU).

Study Overview

Status

Terminated

Conditions

Intervention / Treatment

Detailed Description

Caregivers Consent:

If you agree to take part in this study, you will complete a questionnaire about your opinion on the inpatient occupational therapy session the patient (person you are caring for) received. It should take about 10 minutes to complete the questionnaire. You will be left alone in a room to complete the questionnaire.

Length of Study:

Your participation on this study will be over after you complete the questionnaire.

This is an investigational study.

50 patients and up to 50 caregivers will take part in this study. All will be enrolled at MD Anderson.

Patients Consent:

If you agree to take part in this study, you will complete a questionnaire about your opinion of the inpatient occupational therapy session you just had. The questionnaire should take about 10 minutes to complete. You will be left alone in the room to complete the questionnaire.

Length of Study:

You participation on this study will be over after you complete the questionnaire.

This is an investigational study.

50 patients and up to 50 caregivers will take part in this study. All will be enrolled at MD Anderson.

Study Type

Interventional

Enrollment (Actual)

86

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Houston, Texas, United States, 77030
        • University of Texas MD Anderson Cancer Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Patients must have an inpatient occupational therapy (OT) order and be able to tolerate an OT session as judged by the attending physician
  2. Patients with cancer admitted to inpatient acute palliative care unit
  3. Caregiver participation is optional, but must be identified as the primary caregiver in order to complete the Caregiver Satisfaction Survey.
  4. Caregiver (if participating) must be present during the session.
  5. Patient (and caregiver (if participating) must be 18 years of age or older.
  6. Both patient (and caregiver if participating) must be able to understand, read, write and speak English.
  7. Both patient and caregiver (if participating) must sign an Informed Consent Form.

Exclusion Criteria:

  1. Patients or caregivers with physical limitations (visual or motor impairment) causing inability to read, complete or sign the consent form and survey.
  2. Patients or caregivers who the attending physician deems unable to participate due to poor cognitive capacity or acute physical distress.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Caregiver Questionnaire
Questionnaire completion regarding opinion on the inpatient occupational therapy session person being cared for received.
Questionnaire completion regarding opinion of the inpatient occupational therapy session patient received.
Other Names:
  • Survey
Experimental: Patient Questionnaire
Questionnaire completion regarding opinion of the inpatient occupational therapy session patient received.
Questionnaire completion regarding opinion of the inpatient occupational therapy session patient received.
Other Names:
  • Survey

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction Rate of Inpatient Occupational Therapy Session
Time Frame: 1 day
Satisfaction rate defined as the percentage of patients that "strongly agree" or "agree" after inpatient occupational session as being beneficial.
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Paul W. Walker, MD, M.D. Anderson Cancer Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 13, 2015

Primary Completion (Actual)

January 5, 2020

Study Completion (Actual)

January 5, 2020

Study Registration Dates

First Submitted

August 10, 2015

First Submitted That Met QC Criteria

August 10, 2015

First Posted (Estimate)

August 13, 2015

Study Record Updates

Last Update Posted (Actual)

January 13, 2020

Last Update Submitted That Met QC Criteria

January 8, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 2015-0350

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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