Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06725953

Remote Physical Activity Programming to Improve Outcomes in Cancer Survivors With and Without Type 2 Diabetes

Led by University of Oklahoma · Updated on 2026-05-01

38

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The growing U.S. cancer survivor population is projected to hit 26M by 2040. Chemotherapy represents an effective cancer treatment but can diminish cancer survivors' quality of life-particularly cognitive function-through select pathophysiological processes. Research on chemotherapy-induced cognitive impairment (hereafter, 'chemo-brain') is therefore critical. Chemotherapy disrupts immune system function and antioxidant regulation, causing inflammatory molecule release and damaging the brain's blood vessels. The brain's vascular function and, possibly, its neurons, are subsequently impaired-likely contributing to chemo-brain. Type 2 diabetes (T2D), a common cancer survivor comorbidity, shares underlying pathophysiology with chemo-brain. T2D-related insulin resistance can precipitate repeated high blood sugar episodes which increase inflammatory molecule release. In individuals with T2D without cancer, negative relationships are observed between inflammatory molecule concentrations and the brain's vascular and/or cognitive function. Cancer survivors with T2D might thus have higher chemo-brain risk than those without T2D. Yet, more research must compare how the brain's vascular function, as well as cognitive, inflammatory, and cardiometabolic indices, differ between these groups. Physical activity (PA) counteracts chemo-brain's and T2D's pathophysiology, with higher PA/fitness resulting in better vascular function of the brain, lower inflammatory molecule concentrations, and improved insulin sensitivity. We are therefore conducting a 30-participant quasi-experimental pilot study in cancer survivors with (cases) and without (controls) T2D. We will first investigate between-group differences in the brain's vascular function as well as cognitive, inflammatory, cardiometabolic, and epigenetic outcomes. We will then examine between-group changes in these outcomes and select psychosocial metrics during a 12-week technology-based PA program-potentially further elucidating involved mechanisms.

CONDITIONS

Official Title

Remote Physical Activity Programming to Improve Outcomes in Cancer Survivors With and Without Type 2 Diabetes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Ability to speak and read English
  • Ability to provide informed consent
  • Received chemotherapy treatment for a non-central nervous system cancer within the last three years
  • Self-reported cognitive difficulties following cancer treatment
  • For cancer survivors with type 2 diabetes: current diagnosis confirmed by blood glucose tests or use of diabetes medication
  • For cancer survivors without type 2 diabetes: no current diagnosis confirmed by blood glucose tests
  • Own a smartphone or computer with internet access
  • Willing to participate in a 12-week remote physical activity program
Not Eligible

You will not qualify if you...

  • Physical Activity Readiness Questionnaire (2017 PAR-Q) results indicating physical activity may be unsafe without a doctor's note
  • Engaged in 75 minutes or more of vigorous-intensity or 150 minutes or more of moderate-intensity physical activity per week in the last 3 months
  • Currently a prisoner, pregnant, or planning pregnancy during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Oklahoma Health Sciences

Oklahoma City, Oklahoma, United States, 73104

Actively Recruiting

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Research Team

Z

Zachary C Pope, PhD

CONTACT

M

Mikhail Kellawan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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