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Behavioral Weight Loss Program for Cancer Survivors in Maryland

Behavioral Weight Loss for Overweight and Obese Cancer Survivors in Maryland: A Demonstration Project

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04534309
Acronym
ASPIRE
Enrollment
340
Registered
2020-09-01
Start date
2020-09-22
Completion date
2023-06-30
Last updated
2023-10-10

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

Conditions

Bladder Cancer, Breast Cancer, Endometrial Cancer, Gallbladder Cancer, Kidney Cancer, Melanoma (Skin), Prostate Cancer, Rectal Cancer

Brief summary

Behavioral Weight Loss for Overweight and Obese Cancer Survivors in Maryland: A Demonstration Project

Detailed description

The objective of the ASPIRE Project is to design, implement, and evaluate a real-world, lifestyle-based, support for overweight or obese cancer survivors in both urban and rural areas of Maryland. The project will provide three options of support to encourage lifestyle change to achieve and maintain a healthy weight for cancer survivors: 1. Self-Directed Weight Loss: educational materials only; 2. App-Directed Weight Loss: educational materials, weight loss app with weekly e-mail support; and 3. Coach-Directed Weight Loss: educational materials, weight loss app, weekly e-mail support and one-to-one weekly telephonic coach support.

Interventions

BEHAVIORALWritten Weight Loss Material

Participants will receive written weight loss material by email.

BEHAVIORALWeight Loss App

Participants will receive written weight loss material as well as instructions for using a free weight loss app on their phone or computer.

BEHAVIORALBehavioral Lifestyle Weight Loss Intervention (Coaching)

Participants will receive weekly coaching phone calls to encourage regular dietary, exercise, and self-monitoring practices which encourage gradual, healthy weight loss.

Sponsors

Maryland Cigarette Restitution Fund
CollaboratorOTHER_GOV
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* previously diagnosed with a malignant solid tumor, * completed all required surgical, and/or chemotherapy and/or radiation curative intent therapy at least three months prior to enrollment, * anticipated treatment-free life span of 12 months or longer. * chemoprophylaxis with tamoxifen or aromatase inhibitors for breast cancer in women will be permitted * anti- Luteinizing-hormone releasing therapy for prostate cancer in men will be permitted. * BMI ≥ 25 kg/m2 (BMI ≥ 23 kg/m2 for Asians) and weight ≤ 400 lbs. * have an email address for regular personal use Additional criteria for participants in weight tracking (self-directed or app directed) * willingness to record/transmit quarterly weights for 12 months Additional criteria for App-Directed Program: * willingness to change diet and increase physical activity and track weight, diet and physical activity * have a smart phone for personal use * sufficient data plan/Internet to support daily use of weight loss app\* Additional Criteria for Coach-Directed Weight Loss Program * willingness to lose weight by changing diet and physical activity habits * willingness to track weight, diet and physical activity * willingness to record/transmit quarterly weights for 12 months * smart phone for personal use * data plan/Internet to support daily use of weight loss app\* * willingness to complete coaching calls (12 weekly calls and 3 monthly calls) * sufficient call plan to support coaching calls * a corresponding website could be used, then daily Internet access is required for person use.

Exclusion criteria

* received any chemotherapy (unless anti-hormonal therapy) and/or radiation three months or less prior to the proposed program date * women who are breastfeeding, pregnant, or planning pregnancy within the next year Additional

Design outcomes

Primary

MeasureTime frameDescription
Weight change at 6 months in Coach-Directed ProgramBaseline and 6 monthsEvaluate the effectiveness of the Coach-Directed weight loss programs in a real world setting by examining weight change \[in kilograms (kg)\] at 6-months.

Secondary

MeasureTime frameDescription
Weight change at 6 months in Self-Directed and App-Directed Weight Loss ProgramsBaseline and 6 monthsEvaluate the effectiveness of the Self-Directed and App-Directed weight loss programs in a real world setting by examining weight change \[in kilograms (kg)\] at 6-months.

Other

MeasureTime frameDescription
Program participation as assessed by participant enrollmentEnd of enrollment, up to 2 yearsExamine the enrollment in each program as a measure of program participation.
Adoption of weight loss program activities as assessed by app use frequency6 monthsEvaluate the adoption of the App-Directed Weight Loss Program and Coach-Directed Weight Loss Program by examining app-use frequency at six months.
Implementation of weight loss program as assessed by a participant survey6 monthsEvaluate the implementation of the Coach-Directed Weight Loss Program through a participant survey.
Weight change at 12 months by programBaseline and 12 monthsEvaluate the maintenance of the Self-Directed, App-Directed and Coach-Directed weight loss programs in a real world setting by examining weight change \[in kilograms (kg)\] at 12-months by program.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026