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The MONITOR Study: Remote Monitoring Of a Nutrition Intervention To Optimize Treatment Response

The MONITOR Study: Remote Monitoring Of a Nutrition Intervention To Optimize Treatment Response

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06050395
Enrollment
40
Registered
2023-09-22
Start date
2023-09-12
Completion date
2026-06-01
Last updated
2026-03-31

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

Conditions

Pancreatic Cancer

Brief summary

The purpose of the study is to evaluate the feasibility and acceptability of a remote nutrition coaching and monitoring intervention during the 12-weeks of active chemotherapy for borderline resectable and locally advanced pancreatic cancer participants.

Interventions

BEHAVIORALQuality fo Life Questionnaire (FHSI)

Participants will take a survey at baseline and visit 2 (weeks 6-8), and visit 3 (week 10-14). The Functional Assessment of Cancer Therapy Hepatobiliary Cancer Symptom Index-8 (FHSI) questionnaire uses a 5-point Likert-type scale, 0=not at all and 4=Very much. A lower total score indicates better quality of life.

BEHAVIORALVioscreen Food Frequency Questionnaire (FFQ)

Participants will receive a web-based link and information to complete VioScreen, a web-based food frequency questionnaire, which allows participants to choose the average frequency of consumption of food items over a given time frame (1 month, 3 month, 1 year, etc.) on a Likert scale with choices ranging by individual questions. Total energy and nutrient intake is estimated by summing intakes from each food based on the selected portion size, reported frequency of consumption, and nutrient content of each food item. Anti-inflammatory and pro-inflammatory dietary patterns are calculated using the energy-adjusted dietary inflammatory index (DII) score to represent the inflammatory potential of an individual's overall diet, using data from FFQ responses. Higher DII scores represent more pro-inflammatory diets while lower (i.e., more negative) DII scores represent more anti-inflammatory diet.

Participants will receive educational handouts on diet.

BEHAVIORALNutritionCoaching

Participants will receive bi-weekly nutrition coaching on anti-inflammatory dietary patterns and foods.

Participants will complete a custom exit/follow up survey regarding relevance, acceptability, intervention length and timing, an barriers/facilitators. This survey contains 38 questions scored from 1 -Strongly agree to 5-Strongly disagree. A lower score indicates patient satisfaction with the program and the skills and knowledge gained in the program.

BEHAVIORALFunctional Assessment of Anorexia/Cachexia Treatment (FAACT) Questionnaire

The FAACT questionnaire uses a 5 point Likert-type scale, 0=Not at all, 4=Very much. A higher score indicates better appetite and quality of life.

BEHAVIORALPatient Reported Outcomes Measure- Cognitive Function (PROMIS-Cog) Questionnaire

Participants will complete the PROMIS-Cog form which measures self-reported cognitive deficits. The questionnaire uses a 5 point Likert-type scale, 1=Very often and 5=Never. A higher score indicates higher cognitive function.

Sponsors

H. Lee Moffitt Cancer Center and Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Men or women 18 years of age or more * Newly diagnosed, in place tumors of the pancreas * No documented or observable psychiatric or neurological disorders that would interfere with study participation (e.g., dementia, psychosis) * Able to speak and read English * Able to consume food orally * Chemotherapy naive * Scheduled to receive treatment with chemotherapy * Able to provide verbal informed consent

Exclusion criteria

* Women who are pregnant * Pancreatic cancer not the primary diagnosis * Patients on enteral or parental nutrition * Patients with metastatic pancreatic cancer * Patients with evidence of impeding bowel obstruction * Patients presenting with ascites

Design outcomes

Primary

MeasureTime frameDescription
Recruitment Rate -FeasibilityUp to 8 monthsThe study will be deemed feasible if \>/= 60% of eligible participants are enrolled
Retention Rate - Feasibilityat 12 weeksThe study will be deemed feasible if \>/=70% of participants complete the post-intervention questionnaire
Adherence - Feasibilityat 12 weeksThe study will be deemed feasible if average attendance is \>/=4 weeks of sessions (out of 6) for MONITOR arm

Secondary

MeasureTime frameDescription
Participant Satisfaction with Overall Program- Acceptabilityat 12 weeksThe study will be deemed acceptable based on the satisfaction score on follow-up survey. The follow-up survey uses open-ended and likert-style questions regarding 1) relevance and applicability of the MONITOR intervention content and objective/subjective data collection methods; 2) intervention length and timing; and 3) barriers/facilitators to participation and retention. On a 5-point Lkert-type scale, a(1) =strongly agree and e(5)=strongly disagree. Participant Satisfaction with Overall Program is determined by a score \>/=3 on a 5-point scale.
Participant intent to continue using skills- Acceptabilityat 12 weeksThe study will be deemed acceptable based on the satisfaction score on follow-up survey. The follow-up survey uses open-ended and likert-style questions regarding 1) relevance and applicability of the MONITOR intervention content and objective/subjective data collection methods; 2) intervention length and timing; and 3) barriers/facilitators to participation and retention. On a 5-point Lkert-type scale, a(1) =strongly agree and e(5)=strongly disagree. Participant intent to continue using skills- is determined by a score \>/=3 on a 5-point scale.
Participant perception of utility of knowledge gained - Acceptabilityat 12 weeksThe study will be deemed acceptable based on the satisfaction score on follow-up survey. The follow-up survey uses open-ended and likert-style questions regarding 1) relevance and applicability of the MONITOR intervention content and objective/subjective data collection methods; 2) intervention length and timing; and 3) barriers/facilitators to participation and retention. On a 5-point Lkert-type scale, a(1) =strongly agree and e(5)=strongly disagree. Participant perception of utility of knowledge gained is determined by a score \>/=3 on a 5-point scale.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSylvia Crowder, PhD

Moffitt Cancer Center

PRINCIPAL_INVESTIGATORPamela Hodul, MD

Moffitt Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026