Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
ID07042243

The Florida Partnership for Adding Social Context to Address Cancer Survivorship Outcomes (Florida ASCENT)

Led by University of Florida · Updated on 2026-02-20

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Florida

Lead Sponsor

U

University of Miami

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the MyCarePulse and ASCENT patient navigator intervention to help cancer patients overcome barriers to care, focusing on improving food security, dietary self-efficacy, and diet quality. This study involves patients with colorectal, prostate, lung, breast, gynecologic, hematologic, and skin cancers, including melanoma. The trial is conducted in two phases to adapt, implement, and evaluate the intervention compared to standard care. The study includes a randomized, double-blind design with two groups during phase 2: one receiving the ASCENT patient navigator intervention alongside MyCarePulse, and a comparison group receiving standard care using MyCarePulse alone. Phase 1 involves qualitative interviews with patients and providers to refine the intervention. Phase 2 implements the intervention, with patient navigators connecting flagged patients to resources and support. Participants will complete questionnaires including the U.S. Food Security Survey Module, PROMIS-29, and dietary assessments at baseline and six months. They will also be assessed with the Veggie Meter and participate in interviews. Researchers will measure changes in food security, diet quality, and dietary self-efficacy, as well as health-related quality of life and intervention feasibility. The total study duration includes baseline and six-month follow-up assessments.

CONDITIONS

Brief Title

The Florida ASCENT Study

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Diagnosed with colorectal, prostate, lung, breast, gynecologic, hematologic, or skin (including melanoma) cancer within the past 12 months
  • Able to read and speak English
  • Able to provide informed consent
  • Not considered a vulnerable population such as pregnant women, neonates, or children
Not Eligible

You will not qualify if you...

  • Younger than 18 years old
  • No confirmed diagnosis of the specified cancers within the past 12 months
  • Do not live in the state of Florida
  • Unable to read and speak English or Spanish
  • Unable to provide informed consent
  • Considered a vulnerable population such as pregnant women, neonates, or children

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual) for eligibility assessment

Implementation Strategy (Phase 1)

Duration - Several weeks to months during Phase 1

Participants and community members engage in qualitative interviews and participatory design methods to refine the MyCarePulse platform and ASCENT patient navigator approach.

Multiple visits for interviews and feedback sessions depending on participant engagement

Intervention (Phase 2)

Duration - 6 months

Participants receive either standard care with MyCarePulse or the ASCENT patient navigator intervention to support healthy eating and overcome barriers to care.

Regular interaction with the MyCarePulse platform and patient navigator contacts as needed, with scheduled assessments at baseline and 6 months

Follow-up and Outcome Assessment

Duration - 6 months

Participants complete dietary, food security, self-efficacy, health-related quality of life, and social determinants of health assessments at baseline and 6 months post intervention.

2 visits (baseline and 6 months post-intervention)

Trial Site Locations

Total: 1 location

1

University of Florida

Gainesville, Florida, United States, 32610

Actively Recruiting

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Research Team

D

Dejana Braithwaite, PhD, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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