RECRUITING

Tailored Pain Guide (TPG) Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This research is studying whether changing an individual's behaviors may have an impact as a treatment or outcome for chronic low back pain. This research will try to understand how much an electronic, self-management website like PainGuide can help participants. The study hypothesizes that tailored digital interventions (plus using PainGuide) will demonstrate greater improvement in pain interference.

Official Title

Tailored Pain Guide (TPG) Study

Quick Facts

Study Start:2023-08-18
Study Completion:2025-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05843890

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Chronic Lower Back pain (cLBP) defined by the National Institutes of Health (NIH) Task Force Report on Research Standards for Chronic Low Back Pain, (i.e., low back pain present at least six months, and present more than half of those days.)
  2. * Individuals must have a score of greater or equal to (≥) 60 on PROMIS Pain Interference.
  1. * Current cancer related pain
  2. * Diagnosis of autoimmune disease
  3. * Unable to speak, write or read English
  4. * Visual or hearing difficulties
  5. * Pregnancy or breastfeeding
  6. * Any other diseases or conditions that would make a patient unsuitable for study participation as determined by the site principal investigators.

Contacts and Locations

Study Contact

Beth Banner
CONTACT
734-998-5837
eledward@umich.edu
Sana Shaikh
CONTACT
734-763-5226
skazi@med.umich.edu

Principal Investigator

Daniel Clauw, MD
PRINCIPAL_INVESTIGATOR
University of Michigan

Study Locations (Sites)

University of Michigan
Ann Arbor, Michigan, 48109
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • Daniel Clauw, MD, PRINCIPAL_INVESTIGATOR, University of Michigan

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-18
Study Completion Date2025-02

Study Record Updates

Study Start Date2023-08-18
Study Completion Date2025-02

Terms related to this study

Keywords Provided by Researchers

  • Online resources
  • Fitbit
  • Surveys

Additional Relevant MeSH Terms

  • Chronic Lower Back Pain