Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06725953

Cerebrovascular, Cognitive, Pro-Inflammatory, and Cardiometabolic Outcomes in Cancer Survivors With and Without Type II Diabetes Reporting Chemo-Brain: Baseline Differences and Impact of Activity

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

38

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the effects of chemotherapy on cognitive function, often called "chemo-brain," in cancer survivors, especially those who also have type 2 diabetes (T2D). Chemotherapy can cause immune system disruptions and inflammation that damage brain blood vessels, which may lead to cognitive difficulties. Since T2D shares similar pathophysiological features, cancer survivors with T2D might experience greater cognitive impairments. This study aims to compare brain vascular, cognitive, inflammatory, and cardiometabolic outcomes between cancer survivors with and without T2D. Participants will take part in a 12-week physical activity program delivered remotely through two smartphone applications. This program includes aerobic and resistance exercises supported by a Fitbit activity tracker and resistance bands. The program is designed based on Social Cognitive Theory to promote both physical and psychological health improvements. The study includes 30 cancer survivors divided into two groups: 15 with T2D and 15 without, all self-reporting cognitive difficulties related to chemotherapy. Throughout the study, researchers will assess brain blood flow, vascular resistance, cognitive function, inflammatory markers, and cardiometabolic health at the start and after the 12-week program. Participants will be monitored using questionnaires and biological tests, including blood pressure, glucose levels, and inflammatory molecule concentrations. The study will evaluate how physical activity may impact these measures and improve quality of life for cancer survivors with and without T2D.

CONDITIONS

Brief 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 old or older
  • Ability to speak and read English
  • Ability to provide informed consent
  • Underwent chemotherapy treatment for non-central nervous system cancer within the last three years
  • Self-reported cognitive difficulties following cancer treatment
  • For cancer survivors with type 2 diabetes (CS+T2D): current diagnosis confirmed by blood glucose or HbA1c levels or use of diabetes medication
  • For cancer survivors without type 2 diabetes (CS): no current diagnosis confirmed by blood glucose or HbA1c levels
  • Own a smartphone or computer with internet access
  • Willing to participate in the 12-week remotely-delivered physical activity program
Not Eligible

You will not qualify if you...

  • Physical Activity Readiness Questionnaire score indicating physical activity may be unsafe without a doctor's note
  • Engaged in 75 minutes or more of vigorous physical activity per week, or 150 minutes or more of moderate physical activity per week, in the last 3 months
  • Currently a prisoner
  • Pregnant or planning to become pregnant during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (remote or in-person) to confirm eligibility and collect baseline data

Outpatient Treatment

Duration - 12 weeks

Participants engage in a 12-week remotely delivered physical activity program based on Social Cognitive Theory designed to improve physiological and psychological health outcomes.

Weekly remote interactions via smartphone applications with continuous activity tracking using a Fitbit

Follow-up

Duration - Up to 2 weeks after the program ends

Participants complete post-program assessments to evaluate changes in cerebrovascular function, cognitive function, pro-inflammatory markers, cardiometabolic outcomes, and psychosocial metrics.

1 final remote or in-person visit for outcome assessments

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

M

Mikhail Kellawan, PhD

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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Published Research Related To This Trial

Smartphone-Based Physical Activity Program to Reduce "Chemo-Brain" Symptoms and Improve Health in Cancer Survivors With and Without Type 2 Diabetes: Protocol for a Single-Arm Pre-Post Pilot Trial.

Zachary C Pope, Andriy Yabluchanskiy, Peter Mukli...

https://pubmed.ncbi.nlm.nih.gov/41370824