Benign NeoplasmsNCT02911064
Expectations Regarding Mobility and Self-Care
An observational study of Benign Neoplasms and Malignant Neoplasms of Independent (Primary) Multiple Sites, run by M.D. Anderson Cancer Center at 1 site in United States.
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Benign Neoplasms, Malignant Neoplasms of Independent (Primary) Multiple Sites
- What is being tested?
- Questionnaires
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 133 participants
- Where
- 1 siteUnited States
- Study dates
- 10 Nov 2016to 31 Dec 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Participants scheduled to receive inpatient rehabilitation therapy at University of Texas MD Anderson Cancer Center.
Who may be able to join
- Participants are willing and able to give written informed consent and to comply with all of the study visits and surveys
- Patients with any type of cancer admitted on the acute inpatient rehabilitation unit who can tolerate 3 hours of rehabilitation therapies per day
- Patients 18 years and older
- Patients must be able to understand, read, write, and speak English.
Who cannot join
- Patients who have delirium, severe symptom distress, or cognitive impairment.
- Patients who return to primary service prior to discharge from the acute inpatient rehabilitation unit.
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Texas MD Anderson Cancer Center
Houston, Texas, 77030
About this study
Official title: Assessment of Expectations Regarding Mobility and Self-Care Between Physiatrists and Oncology Patients
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.
Read the detailed 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.
- Being tested
- Questionnaires
- Keywords
- Questionnaires, Surveys, Benign neoplasms, Malignant neoplasms of independent (primary) multiple sites, Inpatient rehabilitation therapy
- Medical subject headings
- Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
QuestionnairesBehavioural
Also called Surveys
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.
| Study group | Role | What they receive |
|---|---|---|
| Assessment 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. Receives: Behavioral: Questionnaires |
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of Participant and Physiatry Practitioner Expectations of Mobility and Activities of Daily Living After Acute Inpatient Rehabilitation Using Barthel Index
Measured: 3 days
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
Measured: 3 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Sep 2016 (estimated)
- Study start10 Nov 2016
- Primary completion31 Dec 2026 (estimated)
- Study completion31 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Benign NeoplasmsStudies of the same condition, open and under way.
- More trials run by M.D. Anderson Cancer CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 133 participants (actual)
Sponsor and investigators
- Lead sponsor
- M.D. Anderson Cancer Center
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Ekta Gupta, MD, Principal investigator, M.D. Anderson Cancer Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02911064
- Sponsor's protocol ID
- 2016-0550
- Other IDs
- NCI-2018-01760
- Status last verified
- Oct 2026
- First submitted
- 16 Sep 2016
- Last updated
- 7 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Assessment of Expectations Regarding Mobility and Self-Care Between Physiatrists and Oncology Patients
- ClinicalTrials.gov ID
- NCT02911064
- Acronym / sponsor ID
- 2016-0550
- Keywords
- Questionnaires, Surveys, Benign neoplasms, Malignant neoplasms of independent (primary) multiple sites, Inpatient rehabilitation therapy
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 133 participants (actual)
- Lead sponsor
- M.D. Anderson Cancer CenterUniversity, hospital or other
- Study start
- 10 Nov 2016 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 31 Dec 2026 (estimated)
- First posted
- 22 Sep 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed 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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Assessment Questionnaires | – | Behavioral: QuestionnairesQuestionnaires 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. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Participants scheduled to receive inpatient rehabilitation therapy at University of Texas MD Anderson Cancer Center.
Key inclusion criteria (4 listed)
- Participants are willing and able to give written informed consent and to comply with all of the study visits and surveys
- Patients with any type of cancer admitted on the acute inpatient rehabilitation unit who can tolerate 3 hours of rehabilitation therapies per day
- Patients 18 years and older
- Patients must be able to understand, read, write, and speak English.
Key exclusion criteria (2 listed)
- Patients who have delirium, severe symptom distress, or cognitive impairment.
- Patients who return to primary service prior to discharge from the acute inpatient rehabilitation unit.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| QuestionnairesAlso: SurveysQuestionnaires 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. | Behavioural | Assessment Questionnaires |
Primary outcome
Assessment of Participant and Physiatry Practitioner Expectations of Mobility and Activities of Daily Living After Acute Inpatient Rehabilitation Using Barthel Index
Time frame: 3 days
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
Time frame: 3 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Oct 2026.
- MD Anderson Cancer CenterLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ekta Gupta, MD principal investigator
M.D. Anderson Cancer Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Benign Neoplasms and Malignant Neoplasms of Independent (Primary) Multiple Sites, run by M.D. Anderson Cancer Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assessment of Participant and Physiatry Practitioner Expectations of Mobility and Activities of Daily Living After Acute Inpatient Rehabilitation Using Barthel Index (time frame: 3 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.