Assessing Exercise Behavior and Preferences Among Patients and Oncologists

August 1, 2023 updated by: Tarah J Ballinger, MD, Indiana University

Assessing Exercise Behavior and Preferences Among Patients and Oncologists at Indiana University Simon Cancer Center

The purpose of this study is to understand the preferences and barriers surrounding exercise of both the patients and oncologists within Indiana University Simon Cancer Center. This information will establish gaps in our current care and provide important information to guide future pilot interventions.

Study Overview

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

Observational

Enrollment (Actual)

60

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

    • Indiana
      • Indianapolis, Indiana, United States, 46202
        • Indiana University Melvin & Bren Simon 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

Sampling Method

Non-Probability Sample

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

    1. Patients with a current or previous diagnosis of stage 0-III or curable solid tumor
    2. Patients receiving any component of their medical oncologic care at IUSCC
    3. Age ≥ 18 years
    4. Able to read and write English

Exclusion Criteria:

  1. Metastatic disease at the time of study participation
  2. Inability to complete the survey

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Subjects
Cancer patients with curable or previously treated malignancies
Survey created at Indiana University to gain information regarding exercise habits, barriers to exercise, and experience with exercise services from the cancer center.
Providers
Physicians seeing patients in the outpatient clinics at the IU Simon Cancer Center
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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of patients who meet exercise recommendations.
Time Frame: baseline
Patients self-reporting more than 150 minutes per week of moderate physical activity OR more than 75 minutes per week of vigorous physical activity
baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient Perceived barriers to exercise during cancer survivorship 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
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

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

Investigators

  • Principal Investigator: Tarah Ballinger, MD, Indiana University

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)

April 8, 2019

Primary Completion (Actual)

February 28, 2020

Study Completion (Actual)

February 28, 2020

Study Registration Dates

First Submitted

August 5, 2019

First Submitted That Met QC Criteria

August 5, 2019

First Posted (Actual)

August 7, 2019

Study Record Updates

Last Update Posted (Actual)

August 3, 2023

Last Update Submitted That Met QC Criteria

August 1, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IUSCC-0690

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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