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Breast Cancer Survivors RESET (Reducing Weight and Elevated Stress Levels Using Educational and Behavioral Tools): A Pilot, Feasibility Study

H. Lee Moffitt Cancer Center and Research Institute logo

H. Lee Moffitt Cancer Center and Research Institute

Status

Active, not recruiting

Conditions

Breast Cancer
Obesity

Treatments

Behavioral: Survivors RESET

Study type

Interventional

Funder types

Other

Identifiers

NCT07101861
MCC-22616

Details and patient eligibility

About

The overall object of this project is to test the feasibility and acceptability of an adapted stress management enhanced behavioral weight loss intervention for Black breast cancer survivors with obesity and elevated stress. We will also conduct pre- and post-intervention assessments of weight, allostatic load, and patient reported outcomes among study participants.

Enrollment

37 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Self-identify as non-Hispanic Black
  • Self-identify as cisgendered female.
  • Are ≥ age 18.
  • Have a history of stage 0-3 breast cancer diagnosis treated for curative intent.
  • Have completed all adjuvant or neoadjuvant chemotherapy, radiation, and surgery at least 21 days prior to study registration but may continue on hormonal therapy and Abemaciclib therapy.
  • Have a measured BMI ≥ 30 kg/m2.
  • Willing to participate for the entire 4-month duration.

Exclusion criteria

  • Are pregnant or are planning to become pregnant during the study period.
  • Have a known major medical or psychological condition known to influence weight loss [e.g., medicated or poorly controlled diabetes (HbA1c > 8%), uncontrolled hypertension (BP>160 mm Hg systolic or BP>100 mm Hg diastolic), cardiovascular event in the past 12 months, history of gastric bypass or bariatric surgery].
  • History of psychiatric hospitalization in past 2 years.
  • History of substance abuse or eating disorder.
  • Any other condition by which a medical professional has suggested diet modification, physical activity, and/or weight loss would be contraindicated.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Sequential Assignment

Masking

None (Open label)

37 participants in 1 patient group

Survivors RESET intervention
Experimental group
Treatment:
Behavioral: Survivors RESET

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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