- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02521194
Occupational Therapy in Palliative Care
Is Inpatient Occupational Therapy Perceived to be Beneficial by the Palliative Patient and Caregiver?
Study Overview
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- University of Texas MD Anderson Cancer Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients must have an inpatient occupational therapy (OT) order and be able to tolerate an OT session as judged by the attending physician
- Patients with cancer admitted to inpatient acute palliative care unit
- Caregiver participation is optional, but must be identified as the primary caregiver in order to complete the Caregiver Satisfaction Survey.
- Caregiver (if participating) must be present during the session.
- Patient (and caregiver (if participating) must be 18 years of age or older.
- Both patient (and caregiver if participating) must be able to understand, read, write and speak English.
- Both patient and caregiver (if participating) must sign an Informed Consent Form.
Exclusion Criteria:
- Patients or caregivers with physical limitations (visual or motor impairment) causing inability to read, complete or sign the consent form and survey.
- Patients or caregivers who the attending physician deems unable to participate due to poor cognitive capacity or acute physical distress.
Study Plan
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:
|
|
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:
|
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
Sponsor
Investigators
- Principal Investigator: Paul W. Walker, MD, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Advanced Cancers
-
M.D. Anderson Cancer CenterCompletedAdvanced CancersUnited States
-
M.D. Anderson Cancer CenterGateway for Cancer Research; Theravalues, Inc.CompletedAdvanced CancersUnited States
-
M.D. Anderson Cancer CenterGE HealthcareWithdrawn
-
M.D. Anderson Cancer CenterCompletedAdvanced CancersUnited States
-
Shanghai Chia Tai Tianqing Pharmaceutical Technology...Recruiting
-
M.D. Anderson Cancer CenterCompleted
-
M.D. Anderson Cancer CenterYukiguni Maitake Company Ltd.Terminated
-
M.D. Anderson Cancer CenterEuropean CommissionCompletedAdvanced CancersUnited States, Spain, France, Israel
-
Aeglea BiotherapeuticsCompletedAdvanced CancersUnited States
-
M.D. Anderson Cancer CenterFoundation MedicineCompleted
Clinical Trials on Questionnaire
-
H. Lee Moffitt Cancer Center and Research InstituteSan Diego State University; University of Minnesota; University of ArizonaCompletedAnxiety | Psychological StressUnited States
-
Centre Hospitalier Universitaire de NiceCompletedGeneral Population | TDAH | Children Aged 5 to 18 YearsFrance
-
Stanford UniversityRecruitingAstigmatism | Nearsightedness | FarsightednessUnited States
-
University Medical Center GoettingenCompletedOrofacial Pain | Sleep ProblemsGermany
-
University of LiegeCompletedCritical Illness | Covid19 | Psychological Stress | FamilyBelgium
-
Imperial College LondonRoyal Marsden NHS Foundation Trust; University College London Hospitals; The... and other collaboratorsCompleted
-
Imperial College Healthcare NHS TrustNot yet recruitingCervical Myelopathy
-
Children's Hospitals and Clinics of MinnesotaCompletedFirearm Injury | Firearm Safety | Firearm OwnershipUnited States
-
Rabin Medical CenterCompleted
-
Fondazione Policlinico Universitario Agostino Gemelli...Recruiting