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A Tailored, Web-Based Self-Management Program to Treat Pain in Chronic Pancreatitis

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University of Michigan

Status

Enrolling

Conditions

Chronic Pancreatitis

Treatments

Behavioral: Web-based self--management program

Study type

Interventional

Funder types

Other

Identifiers

NCT07223554
HUM00277458

Details and patient eligibility

About

This research study aims to evaluate the feasibility and acceptability of a web-based, self-guided, disease-specific self-management program tailored to individual health status profiles for patients with painful chronic pancreatitis.

Full description

This is a single center, prospective, open-label, pilot trial of 30 patients with painful chronic pancreatitis (CP). Participants will be assigned to a 12-week web-based, self-management program known as PainGuide that has been adapted to CP. Participants will receive specific instruction to complete one module a week over the first 4 weeks. Next, participants will receive weekly tailored messaging for the last 8 weeks using symptom scores from baseline assessments and will be asked to complete modules that best address participants symptoms. Participants will complete online surveys at baseline, 4 weeks, 8 weeks, and 12 weeks, and will be interviewed at the end of program to understand participants perceptions on the intervention.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Physician diagnosis of chronic pancreatitis.
  • Abdominal pain for ≥ 3 months and of intensity rated at least 4 or higher on a 0-10 Numeric Rating Scale at least once in the last month.
  • Access to an Internet-connected device (e.g. computer or phone).

Exclusion criteria

  • Unable to speak or read English as the web-based program is currently in English language only.
  • Incarcerated individuals.
  • Currently receiving chemotherapy.
  • Suspected or diagnosed pancreatic cancer.
  • Currently receiving psychotherapy or cognitive behavioral therapy.
  • Serious visual difficulties that would limit completing the web-based program.
  • Substantial cognitive impairment or mental illness that would prevent providing informed consent and completion of questionnaires.
  • Any other condition, which in the opinion of the investigator would impede compliance or hinder the completion of the study.
  • Actively enrolled in another clinical trial for chronic pancreatitis.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Web-based self-management program
Experimental group
Description:
Participants will be assigned to a web-based, self-management program that has been adapted to chronic pancreatitis. Participants will participate in this program for 12 weeks.
Treatment:
Behavioral: Web-based self--management program

Trial contacts and locations

1

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Central trial contact

Angela Theil

Data sourced from clinicaltrials.gov

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