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The Effect of Aerobic Exercise on Selective Biomarkers of Patients With Cancer

The Effect of Supervised Aerobic Exercise on Adipokine and Myokine Biomarkers in Patients With Cancer During Systemic Chemotherapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07048847
Enrollment
32
Registered
2025-07-03
Start date
2022-09-15
Completion date
2023-12-01
Last updated
2025-07-03

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

Conditions

Breast Cancer, Chemotherapy Effect, Colon Cancer

Keywords

Adiponectin, Cancer, Exercise, Irisin, IL-6, Leptin

Brief summary

This study is a single-blinded, prospective, controlled trial aiming to evaluate the effect of supervised aerobic exercise on adipokine and myokine biomarkers in patients with breast or colon cancer during their systemic chemotherapy.

Detailed description

To determine the effect of aerobic exercise on adipokine and myokine biomarkers such as Interleukin-6 (IL-6), Irisin, Leptin and Adiponectin in the blood of breast or colon cancer patients receiving chemotherapy compared to ones who did not exercise during their systemic chemotherapy. Patients who were diagnosed with solid type of cancer specifically focusing on breast or colon cancer will be recruited either to the exercise group (EG) or control group (CG) during their systemic chemotherapy. An individualized supervised resistive aerobic exercise which will be performed via stationary resistive biycle ergometer will be implemented along with the chemotherapy process for EG. Each exercise session will be performed 2 times per week for at least 12 weeks (can be extended up to 24 weeks) during chemotherapy. Exercise intensity will be set as submaximal, 50-70% of heart rate reserve, and each session will be lasted 35 minutes. All exercise sessions will be supervised by the researchers to avoid potential side effects. 5 cc venous blood samples will be collected before the first and last chemotherapy infusions (for both EG and CG). The samples will be blinded to the analyzers did not know which group the samples belonged to.

Interventions

OTHERExercise

The exercise program will be started with 25 Watt (W) for 5 minutes of warm-up. Then it is steadily increased automatically by 5W in 5 minutes apart for 25 minutes for the loading period. The last 5 minutes which will be started by lowering the load to 25 W for cooling will be implemented for cooling down. To prevent acommodation, the warm-up period will be modified by increasing nearly 10% of its previous rate three weeks apart.A submaximal exercise prescription will be followed according to the American College of Sports Medicine guideline by taking into attention 50-70% of Heart Rate Reserve.A submaximal exercise prescription will be followed according to the American College of Sports Medicine guideline by taking into attention 50-70% of Heart Rate Reserve.

Sponsors

Izmir Bakircay University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Having been diagnosed with solid type of cancer * Being candidate for systemic chemotherapy * Being volunteer to participate in an exercise program * Aged between 18-70 years old

Exclusion criteria

* Having 2 or above grades according to the Eastern Cooperative Oncology Group (ECOG) performance status * Having mental and/or cognitive deficits * Ongoing medical and/or surgical (if any) complications * Having neurological/orthopedical and/or severe respiratory dysfunctions * Having any condition which corresponds to the contraindication of exercise (i.e. advanced stages, distant metastasis, infection) * Having unstable vital parameters or having regularly used pharmacological interventions

Design outcomes

Primary

MeasureTime frameDescription
IrisinBaselineMeasuring Serum levels of Irisin via ELISA
LeptinBaselineMeasuring Serum levels of Leptin via ELISA
AdiponectinBaselineMeasuring Serum levels of Adiponectin via ELISA
Interleukin-6 (IL-6)BaselineMeasuring Serum levels of IL-6 via ELISA

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026