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Gepersonaliseerd Oefenprogramma voor Overlevenden van Borstkanker, STEPS-BC Trial (STEPS-BC)

2 oktober 2026 bijgewerkt door: Wake Forest University Health Sciences

Ondersteunend Op Maat Gemaakt Bewegingsprogramma voor Overlevenden van Borstkanker (STEPS-BC)

This clinical trial studies whether a healthy living intervention (HLI), with or without a physical activity intervention (PAI), helps maintain the ability to exercise, heart health, and quality of life in breast cancer patients who are scheduled to receive chemotherapy treatment. Early detection and enhanced therapies for breast cancer have improved 5-year cancer-related survival rates. Unfortunately, many breast cancer survivors are at high risk for long-term exercise intolerance, decreased heart health, and lower quality of life following chemotherapy. Currently, there are no effective therapies to help patients maintain these areas throughout chemotherapy. The HLI in this study includes virtual health education classes, which provide useful information on topics like proper nutrition, managing stress, and sleep practices. This may help patients understand the importance of living a healthy lifestyle during chemotherapy. The PAI in this study consists of virtual exercise sessions personalized to the needs of the patient, which may make it easier for patients to stay active during chemotherapy. HLI with PAI may be a more effective way to help maintain ability to exercise, heart health, and quality of life in breast cancer patients who are scheduled to receive chemotherapy treatment.

Studie Overzicht

Toestand

Werving

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

PRIMARY OBJECTIVES:

I. To determine if a > 10% difference exists in change (i.e., 2.06 ml/kg/min difference) in peak oxygen consumption (VO2) from baseline to 24 weeks after initiating cancer treatment between participants receiving the PAI+HLI versus HLI alone.

II. To determine if a > 10% difference in change in left ventricular ejection fraction (LVEF) from baseline (up to ≤ 4 weeks of chemotherapy initiation) to 24 weeks after initiating cancer treatment exists between participants receiving the PAI+HLI versus HLI alone.

SECONDARY OBJECTIVES:

I. To determine if a > 10% difference in change in LVEF from baseline to 12 weeks after initiating cancer treatment exists between participants receiving the PAI+HLI versus HLI alone.

II. To assess changes in 6-minute walk, health-related quality of life (HRQOL), fatigue, strength, physical activity, sedentary and sitting behaviors and physical function between PAI+HLI and HLI alone groups at baseline to 12 & 24 weeks after initiating cancer treatment.

EXPLORATORY OBJECTIVES:

I. We will examine time-dependent changes in traditional and emerging cardiovascular (CV) disease risk factors, including HRQOL, fatigue, chronic psychosocial stress, objectively-assessed physical activity levels, sedentary and sitting behaviors, 6-minute walk distance, self-efficacy for exercise, plasma lipidomics, pro-inflammatory cytokine and fibrosis biomarkers, left ventricular (LV) injury, heart failure (HF), and social determinants of health on exercise capacity and LVEF.

II. In a subset (n=50), we will use innovative measures of magnetic resonance imaging (MRI) exercise-associated cardiac output (ExCO) and LV myocardial fibrosis with and without gadolinium contrast to examine mechanisms underlying exercise intolerance and LV dysfunction.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM 1: Within three weeks or less of chemotherapy start date, patients access the Trainerize application (app) and attend two virtual pre-chemotherapy exercise sessions over 10-20 minutes each promoting the importance of staying active across the day and throughout treatment and the identification of limitations and familiarization with different types of exercise. Following chemotherapy initiation, patients attend virtual personalized exercise sessions over 20-60 minutes each and organized health workshops over 40 minutes each once a week (QW) during weeks 1-4, once every 2 weeks (Q2W) during weeks 5-16, and once every 4 weeks (Q4W) during weeks 17-24 in the absence of unacceptable toxicity. Patients also receive a Fitbit device, resistance bands, and a loaner tablet, if applicable, on study. Additionally, patients undergo blood sample collection, cardiovascular magnetic resonance imaging (CMR), and cardiopulmonary exercise testing (CPET) on study. Patients may also optionally undergo exercise cardiovascular magnetic resonance imaging (ExeCMR) on study.

ARM 2: Within three weeks or less of chemotherapy start date, patients attend a virtual pre-chemotherapy organized health workshop over 60 minutes. Following chemotherapy initiation, patients attend virtual organized health workshops over 60 minutes each QW during weeks 1-4, Q2W during weeks 5-16, and Q4W during weeks 17-24. Patients also receive a loaner tablet, if applicable, on study. Additionally, patients undergo blood sample collection, CMR, and CPET on study. Patients may also optionally undergo ExeCMR on study.

Studietype

Ingrijpend

Inschrijving (Geschat)

120

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

  • Naam: Karen Craver, MT, MHA
  • Telefoonnummer: 336-716-0891
  • E-mail: NCORP@wfusm.edu

Studie Locaties

  • Verenigde Staten
    • North Carolina
      • Winston-Salem, North Carolina, Verenigde Staten, 27157
        • Werving
        • Wake Forest NCORP RB
        • Contact:
        • Contact:
      • Winston-Salem, North Carolina, Verenigde Staten, 27157
        • Actief, niet wervend
        • Wake Forest NCORP Research Base
    • Virginia
      • Richmond, Virginia, Verenigde Staten, 23235
        • Werving
        • VCU Massey Cancer Center at Stony Point
        • Contact:
        • Hoofdonderzoeker:
          • W. Gregory Hundley, MD
      • Richmond, Virginia, Verenigde Staten, 23298
        • Werving
        • VCU Massey Comprehensive Cancer Center
        • Contact:
        • Hoofdonderzoeker:
          • W. Gregory Hundley, MD
        • Contact:
          • Telefoonnummer: (804) 628-6430.

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 85 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Stage I-III breast cancer (including inflammatory and newly diagnosed, or locally recurrent [if prior treatment received ≥ 2 years prior] but not metastatic breast cancer being treated with curative intent). All molecular subtypes (estrogen receptor [ER], progesterone receptor [PR], human epidermal growth factor receptor 2 [HER2], etc.) are acceptable
  • Scheduled to receive neoadjuvant or adjuvant cytotoxic chemotherapy. Patient must be enrolled ≤ 3 weeks from start of cytotoxic chemotherapy
  • Age 18 to 85 years at enrollment. The upper age cut-off is due to the increased risk of injury in the older population during the CPET, which uses stationary bicycle exercise testing, outweighing the benefit of including this age group
  • Must be able to complete a stationary bicycle exercise test where you pedal against some resistance on a stationary bike with supervisors at your side per patient self-report
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • Able to walk at least 2 blocks without chest pain, dyspnea, shortness of breath or fainting per patient self-report
  • Able to hold breath for 8 seconds
  • Must be able to read and understand English language
  • Must have access to a device that allows teleconferencing (e.g., Zoom calls) or be willing to participate in the Tablet Lending Program
  • Must be willing to download and use the Trainerize application to their personal device or be willing to participate in the Tablet Lending Program
  • Must have a working email address to participate in teleconferencing (e.g., Zoom calls). Local National Cancer Institute Community Oncology Research Program (NCORP) site staff may assist in setting up a new email address, if needed

Exclusion Criteria:

  • At enrollment, the following diagnosis and/or conditions may not be present (i.e., documented in the medical record or by patient self-report):

    • Symptomatic claustrophobia
    • Pregnancy or breast-feeding
    • Ferromagnetic cerebral aneurysm clips or other intraorbital/intracranial metal; pacemakers, defibrillators, functioning neurostimulator devices or other implanted non-compatible MRI devices, such as tissue expanders
    • Uncontrolled hypertension (systolic blood pressure > 190 mm Hg or diastolic blood pressure > 100 mm Hg)
    • Inflammatory conditions such as lupus or inflammatory bowel disease, or another medical condition that might compromise safety or successful completion, as determined by the treating physician
    • Significant ventricular arrhythmias (> 20 premature ventricular contractions [PVCs]/min)
    • Atrial fibrillation with uncontrolled ventricular response (> 130 beats per minute [bpm])
    • Unstable or stable angina (cardiac chest pain)
    • Severe pulmonary hypertension
    • Left main coronary artery disease
    • Symptomatic heart failure
    • Severe valvular heart disease
    • Aortic aneurysm (> 45 mm diameter) or aortic dissection
    • Uncontrolled slow or fast heart rhythm causing symptoms or hemodynamic compromise
    • Hypertrophic obstructive cardiomyopathy

  • Acute myocardial infarction within 28 days of enrollment

  • Acute pulmonary embolus and/or deep vein thrombosis within 24 weeks prior to enrollment

  • Plans to relocate within 6 months of enrollment and unable to participate in study procedures

  • May not be on a simultaneous interventional supportive care (non-therapeutic) clinical trial

  • May not be undergoing simultaneous treatment for a concurrent second primary cancer (patients with historical cancer will not be excluded if chemotherapy was received ≥ 2 years prior)

  • May not be currently engaged in ≥ 300 minutes of moderate to vigorous intensity physical activity per week as determined by self-report on the International Physical Activity Questionnaire -Short Form (IPAQ-SF). Site should use the IPAQ-SF screener in the REDCap WF-2401 STEPS-BC screening project to assist in this determination

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ondersteunende zorg
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Arm 1 (PAI+HLI)

Within three weeks or less of chemotherapy start date, patients access the Trainerize app and attend two virtual pre-chemotherapy exercise sessions over 10-20 minutes each promoting the importance of staying active across the day and throughout treatment and the identification of limitations and familiarization with different types of exercise. Following chemotherapy initiation, patients attend virtual personalized exercise sessions over 20-60 minutes each and organized health workshops over 40 minutes each QW during weeks 1-4, Q2W during weeks 5-16, and Q4W during weeks 17-24 in the absence of unacceptable toxicity. Patients also receive a Fitbit device, resistance bands, and a loaner tablet, if applicable, on study. Additionally, patients undergo blood sample collection, CMR, and CPET on study. Patients may also optionally undergo ExeCMR on study.
Procedure: Biospecimen Collection

Undergo blood sample collection

Andere namen:
  • Biologische monsterverzameling, biologische monsterverzameling, verzamelde biospecimen, biospecimenverzameling, specimenverzameling
Ander: Questionnaire Administration

Ancillary studies

Ander: Exercise Intervention

Attend virtual personalized exercise sessions

Ander: Educational Intervention

Attend organized health workshops

Andere namen:
  • Onderwijs voor Interventie, Interventie door Onderwijs, Interventie door Onderwijs, Interventie, Educatief
Ander: Supportive Care

Receive Fitbit device, resistance bands, and/or loaner tablet

Andere namen:
  • Ondersteunende zorg, ONDERSTEUNENDE ZORG, ondersteunende zorg, Ondersteunende therapie, Symptoombestrijding, Therapie, Ondersteunend
Procedure: Magnetic Resonance Imaging

Undergo CMR

Andere namen:
  • Magnetische Resonantie, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, magnetische resonantie imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging (MRI)
  • Magnetische Resonantiebeeldvorming (procedure), Magnetische Resonantiebeeldvorming Scan, Medische Beeldvorming, Magnetische Resonantie / Nucleaire Magnetische Resonantie, MR, MR, MR Beeldvorming, MRI, MRI, MRI, MRI, MRI, MRI
  • MRI-scan, MRI-scan, MRI-scan, MRI-scan, MRI's, NMR-beeldvorming, NMRI, NMRI, kernspintomografie, Kernspintomografie, sMRI, Structurele MRI
Procedure: Magnetic Resonance Imaging

Undergo ExeCMR

Andere namen:
  • Magnetische Resonantie, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, magnetische resonantie imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging (MRI)
  • Magnetische resonantiebeeldvorming (procedure), Magnetische Resonantiebeeldvorming Scan, Medische Beeldvorming, Magnetische Resonantie / Nucleaire Magnetische Resonantie, MR, MR, MR Beeldvorming, MRI, MRI, MRI, MRI, MRI, MRI, MRI Scan
  • MRI-scan, MRI-scan, MRI-scan, MRI's, NMR-beeldvorming, NMRI, NMRI, nucleaire magnetische resonantiebeeldvorming, Nucleaire Magnetische Resonantiebeeldvorming, sMRI, Structurele MRI
Procedure: Accelerometry

Ancillary Studies

Ander: Electronic Health Record Review

Ancillary Studies

Ander: Cardiopulmonary Exercise Testing

Undergo CPET

Andere namen:
  • CPET, CPX
Actieve vergelijker: Arm 2 (HLI)

Within three weeks or less of chemotherapy start date, patients attend a virtual pre-chemotherapy organized health workshop over 60 minutes. Following chemotherapy initiation, patients attend virtual organized health workshops over 60 minutes each QW during weeks 1-4, Q2W during weeks 5-16, and Q4W during weeks 17-24. Patients also receive a loaner tablet, if applicable, on study. Additionally, patients undergo blood sample collection, CMR, and CPET on study. Patients may also optionally undergo ExeCMR on study.
Procedure: Biospecimen Collection

Undergo blood sample collection

Andere namen:
  • Biologische monsterverzameling, biologische monsterverzameling, verzamelde biospecimen, biospecimenverzameling, specimenverzameling
Ander: Questionnaire Administration

Ancillary studies

Ander: Educational Intervention

Attend organized health workshops

Andere namen:
  • Onderwijs voor Interventie, Interventie door Onderwijs, Interventie door Onderwijs, Interventie, Educatief
Ander: Supportive Care

Receive Fitbit device, resistance bands, and/or loaner tablet

Andere namen:
  • Ondersteunende zorg, ONDERSTEUNENDE ZORG, ondersteunende zorg, Ondersteunende therapie, Symptoombestrijding, Therapie, Ondersteunend
Procedure: Magnetic Resonance Imaging

Undergo CMR

Andere namen:
  • Magnetische Resonantie, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, magnetische resonantie imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging (MRI)
  • Magnetische Resonantiebeeldvorming (procedure), Magnetische Resonantiebeeldvorming Scan, Medische Beeldvorming, Magnetische Resonantie / Nucleaire Magnetische Resonantie, MR, MR, MR Beeldvorming, MRI, MRI, MRI, MRI, MRI, MRI
  • MRI-scan, MRI-scan, MRI-scan, MRI-scan, MRI's, NMR-beeldvorming, NMRI, NMRI, kernspintomografie, Kernspintomografie, sMRI, Structurele MRI
Procedure: Magnetic Resonance Imaging

Undergo ExeCMR

Andere namen:
  • Magnetische Resonantie, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging, magnetische resonantie imaging, Magnetische Resonantie Imaging, Magnetische Resonantie Imaging (MRI)
  • Magnetische resonantiebeeldvorming (procedure), Magnetische Resonantiebeeldvorming Scan, Medische Beeldvorming, Magnetische Resonantie / Nucleaire Magnetische Resonantie, MR, MR, MR Beeldvorming, MRI, MRI, MRI, MRI, MRI, MRI, MRI Scan
  • MRI-scan, MRI-scan, MRI-scan, MRI's, NMR-beeldvorming, NMRI, NMRI, nucleaire magnetische resonantiebeeldvorming, Nucleaire Magnetische Resonantiebeeldvorming, sMRI, Structurele MRI
Procedure: Accelerometry

Ancillary Studies

Ander: Electronic Health Record Review

Ancillary Studies

Ander: Cardiopulmonary Exercise Testing

Undergo CPET

Andere namen:
  • CPET, CPX

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Peak oxygen consumption (VO2)
Tijdsspanne: At baseline and 24 weeks

Will be assessed using cardiopulmonary exercise testing. VO2max, the maximum rate of oxygen consumption measured during incremental exercise, is the gold standard measure of aerobic fitness. It is expressed in milliliters of oxygen consumed per minute per kilogram of body weight (ml/kg/min). Higher VO2max measurements show better function, as it allows one to produce more energy, thereby performing more work.
At baseline and 24 weeks
Left ventricular ejection fraction (LVEF)
Tijdsspanne: At baseline and 24 weeks

Will be assessed using cardiac magnetic resonance imaging (CMR). Left ventricular ejection fraction (LVEF) typically refers to the left side of the heart. It shows how much oxygen-rich blood is pumped out of the left ventricle to most of the body's organs with each contraction. It a percentage, ranging from 0-100%. LVEF helps determine the severity of dysfunction on the left side of the heart. Higher values of LVEF represent better heart function.
At baseline and 24 weeks

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Ejection Fraction (EF)
Tijdsspanne: At baseline and 12 weeks

Will be assessed using cardiac magnetic resonance imaging (CMR). Ejection fraction measures your heart's ability to pump oxygen-rich blood out to your body. In a healthy heart, this is a higher number. A low number means that your heart has difficulty keeping up with your body's needs. It a percentage, ranging from 0-100%. Higher values of EF represent better heart function.
At baseline and 12 weeks
6-minute walk test (6MWT) distance
Tijdsspanne: At baseline, 12 weeks, and 24 weeks.

Will be assessed using the Six Minute Walk Test (6MWT). The 6MWT assesses functional exercise capacity, particularly in individuals with cardiopulmonary conditions. The distance walked in 6 minutes on a flat, straight course, typically 30 meters long, is recorded. The distance reflects submaximal (not peak) exercise capacity. The 6MWT is useful for tracking disease progression, assessing rehabilitation outcomes, and evaluating treatment response. Longer distances in meters represents better exercise capacity.
At baseline, 12 weeks, and 24 weeks.
Physical functioning
Tijdsspanne: At baseline, 12 weeks, and 24 weeks

Will be assessed using grip strength (GS) and Short Physical Performance Battery (SPPB). The SPPB measures lower-extremity function on a 0-12 point scale (higher is better; ≤9 indicates risk, ≤8 indicates impairment). Grip strength, measured by dynamometer, is measured in kgf with higher values representing more strength.
At baseline, 12 weeks, and 24 weeks
Health-related quality of life
Tijdsspanne: At baseline, 12 weeks, and 24 weeks

Will be assessed using the The Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) and FACT-Breast. The Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) scale is a 13-item, self-reported questionnaire designed to measure fatigue severity and its impact on daily activities over the past 7 days. Scores range from 0 to 52, with higher scores indicating less fatigue (better quality of life). A score of less than 30 typically indicates severe fatigue. The Functional Assessment of Cancer Therapy-Breast (FACT-B) is a 44-item self-report questionnaire designed to measure quality of life in breast cancer patients, with total scores ranging from 0 to 148. It comprises the 27-item FACT-General (FACT-G) and a 10-item Breast Cancer Subscale (BCS), focusing on physical, social, emotional, and functional well-being.
At baseline, 12 weeks, and 24 weeks
Physical activity and sedentary behavior levels
Tijdsspanne: At baseline, 12 weeks, and 24 weeks

Will be assessed using ActiGraph and ActivPAL accelerometers including mean daily step count. More steps represent more physical activity and less sedentary behavior.
At baseline, 12 weeks, and 24 weeks
Physical activity levels
Tijdsspanne: At baseline, 12 weeks, and 24 weeks

Physical activity levels will be assessed using the Godin Leisure-Time Exercise Questionnaire (GLTEQ), is a 4-item, self-report tool measuring weekly physical activity frequency across three intensities (strenuous, moderate, light) over a 7-day period. It calculates a total leisure score using 9 (strenuous), 5 (moderate), and 3 (light)-with scores typically classifying individuals as active (≥24 units) or insufficiently active (<24 units). Scores range from 0 with no maximum, higher values represent more physical activity during a week.
At baseline, 12 weeks, and 24 weeks

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Wake Forest University Health Sciences

Onderzoekers

  • Studie stoel: Glenn Lesser, MD, Wake Forest University Health Sciences

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

2 oktober 2026

Primaire voltooiing (Geschat)

30 april 2030

Studie voltooiing (Geschat)

30 april 2030

Studieregistratiedata

Eerst ingediend

11 maart 2026

Eerst ingediend dat voldeed aan de QC-criteria

11 maart 2026

Eerst geplaatst (Werkelijk)

16 maart 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

6 oktober 2026

Laatste update ingediend die voldeed aan QC-criteria

2 oktober 2026

Laatst geverifieerd

1 oktober 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • IRB00144949

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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