RECRUITING

Mood Alterations in the Patients With Non-Muscle Invasive Bladder Cancer Treated With BCG

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

The purpose of this study is to evaluate mood changes in patients with Non-Muscle Invasive Bladder Cancer who are receiving intravesical Bacillus Calmete-Guerin (BCG). Patients with Non-Muscle Invasive Bladder Cancer receiving intravesical treatments are eligible to participate in this study. Participation involves providing research blood and urine samples prior to the start of treatment and throughout the treatment course. The study team will also collect participant's medical history and clinical information. Participants will be asked to complete questionnaires and daily mood diaries.

Official Title

Mood Alterations in the Patients With Non-Muscle Invasive Bladder Cancer Treated With Bacillus Calmete-Guerin

Quick Facts

Study Start:2023-03-21
Study Completion:2028-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05672615

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. * Subjects with a pathologically confirmed non-muscle invasive bladder cancer
  2. * Age ≥ 18 years old
  3. * Ability to understand and willingness to sign a written informed consent document
  1. * Patients that are not candidates for intravesical treatment due to the nature of their disease, such as variant histology or progressive disease after a prior course of intravesical treatment.
  2. * Patients who are pregnant

Contacts and Locations

Study Contact

Riziki Covington
CONTACT
202-660-6133
rcoving5@jh.edu
Armine Smith, MD
CONTACT
202-660-5561
asmit165@jhmi.edu

Principal Investigator

Armine Smith, MD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Sibley Memorial Hospital
Washington, District of Columbia, 20016
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Armine Smith, MD, PRINCIPAL_INVESTIGATOR, Johns Hopkins University

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 Date2023-03-21
Study Completion Date2028-03

Study Record Updates

Study Start Date2023-03-21
Study Completion Date2028-03

Terms related to this study

Keywords Provided by Researchers

  • Bacillus Calmette-Guerin
  • Mood Alterations

Additional Relevant MeSH Terms

  • Non-Muscle Invasive Bladder Cancer