Impact of Routine Electronic Patient-Reported Outcome (ePRO)Symptom Monitoring During Neoadjuvant Therapy in Patients withPancreatic Adenocarcinoma on Patient Experience and ClinicalOutcomes: A Prospective Pre-Post Implementation Study

Part of paid clinical trials in Houston, Texas.

Sponsor
M.D. Anderson Cancer Center
Study ID
NCT07829471
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Standard of Care — OTHER
    Standard of Care

Study Details

To learn if routine symptom monitoring using questionnaires during chemotherapy and/or radiation therapy in patients with PDAC improves patient health-related quality of life and experience with care.

Key Dates

First listed
Sep 21, 2026
Start date
Feb 21, 2027
Status verified
Sep 2026
Primary completion
Jul 1, 2030
Completion
Jul 1, 2032

Study Design

Enrollment
200 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Post-Implementation Cohort
    Standard Clinical Care + QW ePRO
  • Experimental: Pre-Implementation Cohort
    Standard Clinical Care

Primary Outcome Measure

safety and adverse events (AEs) [ Time Frame: Through study completion; an average of 1 year. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UT MD Anderson Cancer CenterHoustonTexas77044
Rebecca A Snyder, MD
[email protected]
713-792-0036
Rebecca A Snyder, MD (PRINCIPAL_INVESTIGATOR)

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By research site
UT MD Anderson Cancer Center· Houston, TX

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