Skip to content

Effects of Activity on Diabetes Risk Among Breast Cancer Survivors on Endocrine Therapy (ABIDE)

The Effects of Cardiorespiratory Fitness, Physical Activity and Sedentary Behavior on Insulin Resistance Among Breast Cancer Survivors Being Treated With Anti-estrogen Endocrine Therapies

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06830486
Acronym
ABIDE
Enrollment
40
Registered
2025-02-17
Start date
2022-02-14
Completion date
2023-10-31
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Exercise, Breast Cancer, Endocrine Therapy, Insulin Resistance, Body Composition

Brief summary

The aim of this study is to learn more about how physical activity and cardiorespiratory fitness are related to diabetes risk among breast cancer patients prescribed an endocrine therapy.

Detailed description

80 women between the ages of 18-80 years will be recruited for this study. The study design consists of two separate in-person visits to University of Colorado Anschutz Medical Campus or Colorado State University. The study consists of glucose testing, a body composition scan, exercise testing, and a two-week period of free living activity monitoring.

Interventions

OTHERNo intervention

No intervention is performed. Participants who have been treated with either a SERM or aromatase inhibitor are recruited and analyzed in separate groups, but the study design for all participants is identical.

Sponsors

University of Colorado, Denver
Lead SponsorOTHER
Colorado State University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Female * diagnosed with breast cancer * age 18-80 years * Completed surgery, chemo- and/or radiation therapy * Prescribed aromatase inhibitor or SERM for at least one year from the time of screening

Exclusion criteria

* Age \< 18 or \> 80 * Type 1 diabetes * Type 2 diabetes * Prescribed anti-hyperglycemic medication, insulin, or sulfonylurea. * Pregnant, breastfeeding or planning to become pregnant in next 2 months * Have absolute contraindications to exercise testing which are: 1. Unstable angina 2. Recent myocardial infarction, cardiac surgery, or vascular surgery (\<3 months) 3. Uncontrolled high blood pressure 4. Heart failure 5. Peripheral artery disease (based on report of symptomatic claudication) 6. Hepatic or renal disease 7. Severe arthritis or mobility impairment that would interfere with exercise testing * Suspected cognitive impairment that would prevent understanding or comprehension of study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Insulin ResistanceImmediately after the consent form is signedInsulin resistance will be measured through oral glucose tolerance testing
Body CompositionImmediately after the insulin resistance measurementBody composition will be measured through DEXA scan
Maximal Exercise CapacityWithin 2-60 days of insulin resistance measurementMaximal exercise capacity measured through graded exercise test on stationary bicycle
Daily Activity2-60 days following insulin resistance measurementDaily activity measured using activity monitor

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRebecca Scalzo, PhD

University of Colorado, Denver

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026