Skip to main content
TTrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor.
RECRUITINGPhase 4INTERVENTIONAL

Studying the Relationship of Patient Positioning and Intravesical Bacillus Calmette Guerin Dwell Time to Improve the Treatment of Non-muscle Invasive Bladder Cancer

An Assessment of Patient Position and Intravesical BCG Dwell Time

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This phase IV trial studies whether there is a relationship between how a patient is positioned while receiving bacillus Calmette Guerin (BCG) within the bladder (intravesical) and how long BCG stays in the bladder (dwell time) to improve the treatment of non-muscle invasive bladder cancer. For the past 40 years, intravesical BCG has been used for the treatment of non-muscle invasive bladder cancer. An important factor for BCG treatment is the dwell time, which is the period of time a patient can hold the BCG medication in the bladder after it has been given. Normally, patients are instructed during intravesical BCG treatment to avoid emptying the bladder for 2 hours after the BCG is given. However, this may be difficult for some patients who may have limited bladder capacity, restricted movement, or severe urinary symptoms. There have been studies outlining the relationship with increased dwell time and how well the treatment works, but studies on the potential impact of patient positioning or activity on the patient's ability to retain the drug are limited. Researchers hope by studying whether there is a relationship between patient positioning during intravesical BCG treatment and dwell time, they may be able to improve how BCG treatment for non-muscle invasive bladder cancer is given, especially for patients with limited bladder capacity, restricted movement, or severe urinary symptoms.

Who May Be Eligible (Plain English)

Who May Qualify: - Patient with intermediate or high risk NMIBC opting for intravesical induction BCG - Has not initiated induction therapy - Able to remain in supine position for two hours. (Head may be raised on up to two pillows) - Able to remain in a sitting position for two hours - Willingness to utilize a wearable fitness tracker for at least five days during the study - Able to perform a remote video or telephone encounter - Able to provide willing to sign a consent form Who Should NOT Join This Trial: - Receipt of intravesical BCG within the past 1 year - Known inability to retain BCG - History of urinary incontinence with a score of 3 or more on the Overactive Bladder Survey (OAB) urgency, urgency incontinence, or incontinence questions - Refusal to wear a fitness tracker during a 24-hour baseline, during treatment, and/or for 2 hours post treatment Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patient with intermediate or high risk NMIBC opting for intravesical induction BCG * Has not initiated induction therapy * Able to remain in supine position for two hours. (Head may be raised on up to two pillows) * Able to remain in a sitting position for two hours * Willingness to utilize a wearable fitness tracker for at least five days during the study * Able to perform a remote video or telephone encounter * Able to provide informed consent Exclusion Criteria: * Receipt of intravesical BCG within the past 1 year * Known inability to retain BCG * History of urinary incontinence with a score of 3 or more on the Overactive Bladder Survey (OAB) urgency, urgency incontinence, or incontinence questions * Refusal to wear a fitness tracker during a 24-hour baseline, during treatment, and/or for 2 hours post treatment

Treatments Being Tested

PROCEDURE

Accelerometry

Receive and wear Fitbit

BIOLOGICAL

BCG Solution

Given intravesically with no activity restrictions

BIOLOGICAL

BCG Solution

Given intravesically in lying down position

BIOLOGICAL

BCG Solution

Given intravesically in sitting position

OTHER

Electronic Health Record Review

Ancillary studies

BEHAVIORAL

Patient Discharge

Receive immediate clinic discharge

OTHER

Survey Administration

Ancillary studies

Locations (1)

Ohio State University Comprehensive Cancer Center
Columbus, Ohio, United States