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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02911064
Other study ID # 2016-0550
Secondary ID NCI-2018-01760
Status Active, not recruiting
Phase
First received
Last updated
Start date November 10, 2016
Est. completion date December 31, 2026

Study information

Verified date May 2024
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this research study is to learn if there is a difference between your expectations of how well you will perform daily living activities after short-term inpatient rehabilitation and the doctor's expectations of how well you will perform daily living activities.


Description:

If you agree to take part in this study, you will complete questionnaires before your inpatient rehabilitation and after you complete inpatient rehabilitation. The questionnaires will ask about how well you currently perform daily living activities, your expectation of how well you will perform daily living activities after you complete inpatient rehabilitation, your symptoms in the past 24 hours, and your physical, functional, social, and emotional well-being. These questionnaires should take about 15 minutes total to complete. Information from your medical record (such as your age, gender, religion, cancer diagnosis, stage of cancer, and so on) will be collected. Length of Study: You participation on this study will be over after you complete the questionnaires. This is an investigational study. Up to 111 participants will take part in this study. All will be enrolled at MD Anderson.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 133
Est. completion date December 31, 2026
Est. primary completion date December 31, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Participants are willing and able to give written informed consent and to comply with all of the study visits and surveys 2. Patients with any type of cancer admitted on the acute inpatient rehabilitation unit who can tolerate 3 hours of rehabilitation therapies per day 3. Patients 18 years and older 4. Patients must be able to understand, read, write, and speak English. Exclusion Criteria: 1. Patients who have delirium, severe symptom distress, or cognitive impairment. 2. Patients who return to primary service prior to discharge from the acute inpatient rehabilitation unit.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Questionnaires
Questionnaires completed before and after inpatient rehabilitation. Questionnaires ask about daily living activity performance, expectation of how well daily living activities will be performed after completion of inpatient rehabilitation, symptoms experienced in the past 24 hours, and physical, functional, social, and emotional well-being. These questionnaires should take about 15 minutes total to complete.

Locations

Country Name City State
United States University of Texas MD Anderson Cancer Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of Participant and Physiatry Practitioner Expectations of Mobility and Activities of Daily Living After Acute Inpatient Rehabilitation Using Barthel Index 3 days
Primary Assessment of Participant and Physiatry Practitioner Expectations of Mobility and Activities of Daily Living After Acute Inpatient Rehabilitation Using Eastern Cooperative Oncology Group (ECOG) Performance Status Scales 3 days
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