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BfedBwell Program for Cancer Survivorship

MM
Overseen ByMelissa Mamele, MS, RD, CSCS
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Colorado, Denver
Must not be taking: Appetite suppressants, Lithium, Antipsychotics, others
Disqualifiers: Diabetes, Cardiovascular disease, Severe depression, others
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This single-arm pilot study will evaluate the feasibility and acceptability of a comprehensive survivorship lifestyle intervention addressing nutrition, exercise, sleep health, and stress management. The intervention integrates the BfedBwell survivorship nutrition program with the BfitBwell clinical exercise oncology program. The augmented BfedBwell program includes: (1) a core education curriculum, (2) 1:1 counseling with a registered dietitian, (3) behavioral skills development, (4) group support, and (5) commercially available wearable technology and smart scales for self-monitoring of physical activity, sleep, and body weight.

Who Is on the Research Team?

EH

Emily Hill, PhD, RDN

Principal Investigator

University of Colorado, Denver

Are You a Good Fit for This Trial?

Inclusion Criteria

I finished active cancer treatment 3 months to 10 years ago or am on long-term maintenance therapy.
* Have a primary care provider (or are willing to establish care with a primary care provider prior to study enrollment) to address medical issues which may arise during screening or study procedures/interventions and who will provide clearance to participate in a nutrition and exercise program
* Ability and willingness to participate in a supervised exercise program; with ability assessed by the Physical Activity Readiness Questionnaire (PAR-Q+) and questions based upon National Comprehensive Cancer Network (NCCN) guidelines (note: any positive responses will trigger a required physician clearance form)
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention

Participants receive a 6-month comprehensive survivorship lifestyle intervention combining nutrition education and counseling with structured exercise programming.

24 weeks
Weekly sessions

Follow-up

Participants are monitored for changes in sleep quality, perceived stress, and physiological indicators of stress and immune function.

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • BfedBwell INSPIRE Pilot

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: BfedBwell INSPIRE InterventionExperimental Treatment6 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Colorado, Denver

Lead Sponsor

Trials
1,842
Recruited
3,028,000+

American Institute for Cancer Research

Collaborator

Trials
12
Recruited
8,600+

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