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Active, Not Recruiting

NCT Number: NCT05132296

Mobile-Health Delivery of Lifestyle Interventions for Women With Breast Cancer

This clinical trial aims to develop a lifestyle program to improve clinical outcomes in women with breast cancer who do not have a healthy diet, regular exercise habits, or ways to manage their stress well. The program will include support and counseling in healthy eating, physical activity, stress management and mindfulness, learning sleep hygiene techniques, and behavioral counseling in addition to social support. Developing a lifestyle program may help improve quality of life and encourage healthy lifestyle choices among patients diagnosed with breast cancer.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Wake Forest University Health Sciences, Winston-Salem, North Carolina, United States

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About this study

PRIMARY OBJECTIVE:

I. Assess the feasibility of delivering a mobile, standardized, comprehensive lifestyle program in women with breast cancer (BCa).

SECONDARY OBJECTIVES:

I. Determine whether the comprehensive lifestyle intervention program (CLIP) group has reduction in body mass index (BMI) and percent body fat and weight over time.

II. Determine whether the CLIP group has improved outcomes in anthropometric measures, dietary patterns, and fitness measures and patient-reported outcomes including quality of life (QOL), fatigue, sleep disturbances, mental health, social support, and mindfulness.

OUTLINE: Patients are randomized into 1 of 2 groups.

GROUP I: Patients undergo 60 minute sessions of nutrition education for 12 weeks and behavioral intervention 26 weeks. Patients receive FitBit and undergo physical activity for 30-60 minutes 5 days a week (aerobic activity) and 2 days a week (resistance training).

GROUP II: Patients have access to all usual care supportive services.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women with stage I-III BCa scheduled to undergo radiation therapy (RT) or within the first 12 months of having completed primary treatment (they do not need to have undergone RT)
  • Underwent chemotherapy and surgery
  • Able to read, write, and speak English
  • BMI of 25 or higher
  • 18 years of age or older
  • Oriented to person, place, and time
  • Participants must meet at least two of the following criteria related to their lifestyle at the time of diagnosis:
  • Consume less than 3 servings of fruit and vegetable/day
  • Engage in less than 75 minutes of moderate/vigorous intensity activity per week, defined as anything that causes small increases in breathing or heart rate for a sustained amount of time (e.g., brisk walking, bicycling)
  • Engage in a mind-body practice less than 4 times a month
  • Access to internet connection
  • Access to a tablet, laptop or computer
  • Able to come to University of Texas (UT) MD Anderson or Wake Forest for blood collection
  • Able to perform light physical activity. if any medical issues exist or arise that may limit performing physical activity, a medical release will be required

Exclusion criteria

  • Have not completed chemotherapy; have a recurrent BCa diagnosis; another primary cancer diagnosis within past 5 years (not including non-melanoma skin cancers)
  • Any major thought disorder (e.g., schizophrenia, dementia)
  • Any major communication barriers that would preclude being able to complete the intervention (e.g., visually or hearing impaired)
  • Poorly or uncontrolled diabetes in the opinion of the physician(s)
  • Extreme mobility issues (e.g., unable to get in and out of a chair unassisted)

Treatment and study plan

behavioral intervention

Behavioral

Undergo behavioral counseling

Other names: Behavior Conditioning Therapy, Behavior Modification, Behavior or Life Style Modifications, Behavior Therapy, Behavioral Interventions, Behavioral Modification, Behavioral Therapy, Behavioral Treatment, Behavioral Treatments

Best Practice

Other

Receive usual care supportive services

Other names: standard of care, standard therapy

Fitbit

Device

Receive FitBit

Nutrition Education

Behavioral

Receive nutrition education

Physical activity

Other

Undergo physical activity

Questionnaire Administration

Other

Ancillary studies

Primary outcomes

  1. Assess the feasibility of delivering a mobile, standardized, comprehensive lifestyle program in women with BCa.

    Time frame: up to 9 months after study baseline

    The feasibility criteria will include consent rate (how many patients are consented in a period of time), adherence rate ( how many patients adhere to the program and finish it), and study retention rate ( how many patients that are consented stay with the program until the end/ low number of participants withdrawing from the study after consent).

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Mobile-Health Delivery of Lifestyle Interventions for Women With Breast Cancer Multicenter Pilot Trial

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Nov 24, 2021
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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