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Clinical Trials/NCT05687604
NCT05687604
Recruiting
Not Applicable

Scalable TELeheaLth Cancer CARe: The STELLAR Program to Treat Cancer Risk Behaviors

Northwestern University1 site in 1 country1,500 target enrollmentSeptember 24, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Northwestern University
Enrollment
1500
Locations
1
Primary Endpoint
Reach/Access
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

The goal of this clinical trial is to improve cancer patient's health, survival, and quality of life by dispelling risk behaviors for Northwestern Memorial Health Care (NMHC) patients who are cancer survivors.

The main question[s] STELLAR aims to answer are:

  • How best to combine three behavior interventions (physical activity promotion, smoking cessation, obesity treatment) into one treatment.
  • Evaluate the reach of the program. We will look at the number, proportion, and representativeness of participants in terms of disease characteristics, socioeconomic status, telehealth readiness, and race/ethnicity.
  • Evaluate the effects of the STELLAR program relative to enhanced usual care (information provision) on cancer risk behaviors, patient care access, care quality, and communication.

Participants will be provided goals related to their physical activity, smoking, and/or weight loss and asked to track their health behaviors via an app, excel file, or on paper. At baseline, 3 months, 6 months and 9 months into the study, participants will provide survey responses and physical measurements like height and weight. Additionally, those in the Facilitated group will complete 12 telehealth sessions with study staff to discuss progress towards their study goals.

Researchers will compare the Facilitated group to the Self Guided group to see if the Facilitated intervention group is able to reach more participants that enhances care only.

Detailed Description

The goal of this clinical trial is to decrease adverse outcomes and improve cancer patient's health, survival, and quality of life by dispelling risk behaviors for Northwestern Memorial Health Care (NMHC) patients. The main question\[s\] STELLAR aims to answer are: * How best to combine three existing effective cancer risk behavior interventions (physical activity promotion, smoking cessation, obesity treatment) into one treatment program within the existing NMHC environment. * Evaluate the reach of the FACILITATED program. We will look at the number, proportion, and representativeness of individuals who are willing to participate in terms of disease characteristics, socioeconomic status, telehealth readiness, and race/ethnicity. * Evaluate the effects of the FACILITATED program relative to enhanced usual care (information provision) on cancer risk behaviors, patient care access, care quality, healthcare utilization, patient-provider communication, cost and health outcomes (symptoms and quality of life). Participants will be recruited through several channels (MyNM, direct outreach from research staff, EDW). Interested patients will then be randomly assigned to the STELLAR program arm, or Enhanced Usual Care. Participants in the STELLAR program will be enrolled for a year into the program. Participants will be provided goals related to their physical activity, smoking, and/or weight loss and asked to track their health behaviors via an app, excel file, or on paper. At baseline, 3 months, 6 months and 9 months into the study, participants will provide survey responses and physical measurements like height and weight. Additionally, those in the FACILITATED group will complete 12 telehealth sessions with study staff to discuss progress towards their study goals. Researchers will compare the FACILITATED intervention group to the SELF GUIDED group to see if the FACILITATED intervention group is able to reach more participants that Self Guided only.

Registry
clinicaltrials.gov
Start Date
September 24, 2024
End Date
July 31, 2027
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brian Hitsman

Associate Professor of Preventive Medicine

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Northwestern Medicine patient
  • Over 18 years old
  • Meet at least 1 of the following 3 criteria:
  • Engage in \<150 min/week of physical activity
  • BMI of ≥25
  • Report that they currently smoke or smoked within the last year
  • Diagnosed with any cancer (except non-melanoma skin)
  • Ability to attend telehealth visits either via landline, cell phone, smartphone, tablet, laptop, or desktop computer
  • 3 months post curative intent treatment if BMI of ≥25 or engage in \<150 min/week of physical activity
  • Post curative intent treatment if they currently smoke or smoked within the last year

Exclusion Criteria

  • Currently in another dietary, weight loss, smoking cessation (including cessation pharmacotherapy), or physical activity treatment/intervention.
  • Limited level of oral and written English or Spanish
  • Cognitively impaired adults
  • Prisoners
  • Participants will be excluded from the physical activity and weight loss interventions (but not the smoking cessation component) for:
  • Absolute contraindications to exercise (i.e., acute myocardial infarction, complete heart block, acute congestive heart failure, unstable angina, uncontrolled hypertension), metastatic disease or planned elective surgery
  • Pregnant or plans to become pregnant.
  • Individuals engaging in the physical activity or weight loss interventions must pass pre- physical activity participation screening or obtain medical clearance

Outcomes

Primary Outcomes

Reach/Access

Time Frame: Baseline

A) We will evaluate the Reach of the risk behavior screening system by assessing the number of cancer survivors exposed to EHR screening and the proportion and representativeness of those who enroll in the study and are randomized. B) We will also evaluate the Reach of the STELLAR intervention by assessing the proportion and representativeness (in terms of disease characteristics, socioeconomic status, telehealth access, technology literacy, race/ethnicity, and insurance status) of those randomized to active intervention who attend at least one treatment session.

Secondary Outcomes

  • Godin Leisure Time Exercise Questionnaire(baseline, 3, 6 and 9 months)
  • Smoking(baseline, 3, 6 and 9 months)
  • Body Weight(baseline, 3, 6 and 9 months)
  • Self-Reported Weekly Amount (in days and minutes) of Moderate Intensity Physical Activity(baseline, 3, 6 and 9 months)
  • Total Healthcare Cost and Amount of Patient Care Utilization(baseline, 3, 6 and 9 months)
  • Rating of Care Quality as Measured by the Consumer Assessment of Healthcare Providers & Systems Cancer Care Survey)(baseline, 3, 6 and 9 months)
  • Rating of Patient-Provider Communication and Shared Decision-Making as Measured by The Interpersonal Process of Care (IPC32)(baseline, 3, 6 and 9 months)
  • Rating of Symptoms and Functioning as Measured by the Patient-Reported Outcomes Measurement Information System (PROMIS-29) Profile(baseline, 3, 6 and 9 months)
  • Rating of Quality of Life Using the Health Related Quality of Life Short Form (HRQOL SF-12)(baseline, 3, 6 and 9 months)

Study Sites (1)

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