Early Supportive Care and Nutritional Support in Adults With Pancreatic Cancer

NCT05438927 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2026-03-31

No results posted yet for this study

Summary

The purpose of the study is to assess the feasibility and patient satisfaction with the Support through Remote Observation and Nutrition Guidance (STRONG) program. The program provides nutrition and supportive care for participants living with pancreatic cancer who are receiving chemotherapy.

Conditions

Interventions

BEHAVIORAL

Fitbit Data Collection

Participants will log food intake while sharing their data with a dietician in real time for 12 weeks

BEHAVIORAL

Nutrition Counseling

Participants will receive individually tailored, biweekly nutrition counseling from a dietician via telehealth

BEHAVIORAL

Fact G Survey

Participants will take a survey at baseline and weeks 4,8,12 \& 16. The questionnaire includes questions about participant's physical, social, emotional and functional well being over the past 7 days. This questionnaire uses a 5 point Likert-type scale, 0=not at all, 4=very much. A higher total score indicates better quality of life.

BEHAVIORAL

General Anxiety Disorder (GAD)-7

Participants will take a survey at baseline and weeks 4,8,12 \& 16. The questionnaire measures participants anxiety with a scale of 0=not at all, 3=Nearly everyday.

BEHAVIORAL

Patient Health Questionnaire (PHQ)-9

Participants will take a survey at baseline and weeks 4,8,12 \& 16. The questionnaire measures participants depression with a scale of 0=not at all, 3=Nearly everyday.

Sponsors & Collaborators

  • Canopy Cancer Collective

    collaborator UNKNOWN
  • H. Lee Moffitt Cancer Center and Research Institute

    lead OTHER

Principal Investigators

  • Amir Alishahi Tabriz, MD, PhD · Moffitt Cancer Center

  • Pamela Hodul, MD · Moffitt Cancer Center

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-15
Primary Completion
2024-10-16
Completion
2025-09-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05438927 on ClinicalTrials.gov