- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04047589
Assessing Exercise Behavior and Preferences Among Patients and Oncologists
Assessing Exercise Behavior and Preferences Among Patients and Oncologists at Indiana University Simon Cancer Center
Study Overview
Status
Conditions
Detailed Description
This descriptive, cross-sectional study will survey patients with a current or previous diagnosis of non-metastatic solid tumor malignancy who are being seen at the Indiana University Simon Cancer in Indianapolis, Indiana. Patients with active, incurable disease are excluded. Willing and eligible patients will complete a brief, 14 question survey while seen in the waiting room of the women's or multi-disciplinary clinics. We aim to survey 350 patients over a 12 month period. Patients will fill out the survey at only one point in time and no patient identifiers will be kept.
During COVID-19 restrictions, we will also send out an electronic version of the survey to participants using the email address provided in their Cerner accounts. Responses will be captured by REDCAP and will remain anonymous and not linked to the patients' medical record or personal health information.
The physician survey will be emailed to oncologist/hematologists practicing within IUSCC who see patients at least once per week. Physicians will receive a survey at only one point in time. The survey will be anonymous and no physician identifiers will be kept.
Primary objective Estimate the proportion of patients with curable solid tumor malignancies seen at the Indiana University Simon Cancer Center who are meeting exercise recommendations for cancer survivors (more than 150 minutes per week of moderate or 75 minutes per week of vigorous activity).
Secondary objectives
- Assess patients' perceived barriers to exercise during cancer survivorship
- Assess patients' preferences for receiving exercise recommendations
- Assess oncologists' perceived barriers to making exercise recommendations
- Assess oncologists' preferences for exercise and physical activity resources that could be provided by the cancer center
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Indiana
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Indianapolis, Indiana, United States, 46202
- Indiana University Melvin & Bren Simon Cancer Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Potential patients will be identified in the outpatient clinics (women's and multi-disciplinary) at the IU Simon Cancer Center. Physicians will be given the option of requesting that their patients not participate in the survey. When patients check in or are placed in an exam room, a trained member of the clinic staff will approach patients about possible participation in the survey study.
Physicians seeing patients more than once per week in the outpatient clinics at the IU Simon Cancer Center will receive email invitation to participate in the survey. An online survey will be administered via Survey Monkey. This does not require an informed consent process. The survey has 14 questions and will take approximately 5 minutes to complete.
Description
Inclusion Criteria:
- Physician survey Any oncologist/hematologist practicing within IUSCC regularly providing care for patients with solid tumor malignancies (seeing patients one or more days per week in the multidisciplinary or women's clinics with solid tumor malignancies). Physicians providing care only for hematologic (multiple myeloma, leukemia, lymphoma, transplant) or benign disorders will be excluded.
Patient survey
- Patients with a current or previous diagnosis of stage 0-III or curable solid tumor
- Patients receiving any component of their medical oncologic care at IUSCC
- Age ≥ 18 years
- Able to read and write English
Exclusion Criteria:
- Metastatic disease at the time of study participation
- Inability to complete the survey
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Subjects
Cancer patients with curable or previously treated malignancies
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Survey created at Indiana University to gain information regarding exercise habits, barriers to exercise, and experience with exercise services from the cancer center.
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|
Providers
Physicians seeing patients in the outpatient clinics at the IU Simon Cancer Center
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Survey regarding personal exercise habits and beliefs, barriers to making exercise recommendations, and potential resources the cancer center might provide to help make effective exercise recommendations in the future
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of patients who meet exercise recommendations.
Time Frame: baseline
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Patients self-reporting more than 150 minutes per week of moderate physical activity OR more than 75 minutes per week of vigorous physical activity
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baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Perceived barriers to exercise during cancer survivorship via pilot survey
Time Frame: Baseline
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Investigator created survey with 14 items regarding demographics, cancer history, exercise habits, and exercise as part of cancer treatment
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Baseline
|
|
Patient preferences for receiving exercise recommendations via pilot survey
Time Frame: Baseline
|
Investigator created survey with 14 items regarding demographics, cancer history, exercise habits, and exercise as part of cancer treatment
|
Baseline
|
|
Provider perceived barriers to making exercise recommendations via pilot survey
Time Frame: Baseline
|
Investigator created survey with 14 items regarding demographics, cancer speciality, exercise habits, and exercise recommendations to patients and patient exercise habits
|
Baseline
|
|
Provider preferences for exercise and physical activity resources that could be provided by the cancer center via pilot survey
Time Frame: Baseline
|
Investigator created survey with 14 items regarding demographics, cancer speciality, exercise habits, and exercise recommendations to patients and patient exercise habits
|
Baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tarah Ballinger, MD, Indiana University
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IUSCC-0690
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.
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