Initiative to Minimize Disparities in Postoperative Prostate Cancer Care

NCT ID: NCT03755492

Last Updated: 2022-07-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

24 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-01

Study Completion Date

2022-07-20

Brief Summary

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Einstein Healthcare Network in North Philadelphia serves a predominantly underserved medical community. The investigators routinely see patients who cannot afford absorbent pads after prostate surgery, which helps with quality of life secondary to urinary incontinence. The investigators will provide absorbent pads to participants who would be unable to afford them. The investigators hypothesize that providing absorbent pads for 6 months will result in improved quality of life in regards to management of urinary incontinence after radical prostatectomy.

Detailed Description

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When detected early and managed with appropriate surgical treatment, such as radical prostatectomy, Prostate cancer prognosis is excellent, but recovery may be associated with significant transient impact on quality of life. This impact most often manifests in urinary domains, specifically, development of stress urinary incontinence. Several simple, low-cost but high-yield interventions may dramatically improve patient's postoperative quality of life. However, such interventions may be out of reach for patients from Health Enterprise Zones (HEZ) with limited funds. To make resources readily available for this patient population, the inclusion criteria will be prostatectomy patients of any age who reside within the designated North Broad street HEZ.

Stress urinary incontinence after prostatectomy is a source of major distress. Incontinence tends to improve over time with most patients regaining their urinary function. Symptomatic support with disposable absorbent pads/diapers for several months helps men effectively manage this side effect. While for most men the cost of the diapers is manageable, for men in HEZ this represents a significant financial burden on the patient and on caregivers. As a result, these patients often choose to remain home bound until they recover urinary control, preventing them from early return to employment and resulting in social isolation. The Healthcare Disparity SEED Grant will provide up to a 6-month supply of disposable absorbent pads/diapers to those patients meeting our inclusion criteria. Michigan Incontinence Symptom Index (M-ISI) questionnaires will be distributed to patients pre-operatively and during interval post-operative office visits to assess patient satisfaction with voiding function.

In addition to distributing M-ISI questionnaires, we will also distribute the Extended Prostate Cancer Index Composite for Clinical Practice (EPIC-CP) to evaluate overall quality of life. This is a validated questionnaire capable of accurately assessing multiple domains of quality of life after prostate cancer treatment. Results of M-ISI and EPIC-CP scores will be compiled and analyzed to determine if intervention has resulted in measurable improvement between the treatment and control groups.

Conditions

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Post Prostatectomy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Group 1 (Provided absorbent pads)

Patients will receive a 6 month supply (as needed) of absorbent pads for urinary incontinence.

Absorbent pad for urinary incontinence

Intervention Type OTHER

6 month supply provided to patients as needed for urinary incontinence after radical prostatectomy

Group 2 (not provided absorbent pads)

Patients enrolled in the control arm will not receive absorbent pads.

No interventions assigned to this group

Interventions

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Absorbent pad for urinary incontinence

6 month supply provided to patients as needed for urinary incontinence after radical prostatectomy

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. History of prostate cancer
2. Scheduled for radical prostatectomy during a designated academic year
3. Reside within Health Enterprise Zone (HEZ) of North Broad Street
4. Median annual household income \< $50,000
5. Patient feels that they would struggle to afford absorbent pads and Tadalafil based on their annual income
6. Patient must have no history of stress urinary incontinence prior to surgery

3. Patients with cognitive impairment will be excluded from the study
Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Albert Einstein Healthcare Network

OTHER

Sponsor Role lead

Responsible Party

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Serge Ginzburg, MD

Urologic Oncologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Serge Ginzburg, M.D.

Role: STUDY_DIRECTOR

Einstein Healthcare Network

Locations

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Albert Einstein Healthcare Network

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

References

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Suskind AM, Dunn RL, Morgan DM, DeLancey JO, McGuire EJ, Wei JT. The Michigan Incontinence Symptom Index (M-ISI): a clinical measure for type, severity, and bother related to urinary incontinence. Neurourol Urodyn. 2014 Sep;33(7):1128-34. doi: 10.1002/nau.22468. Epub 2013 Aug 14.

Reference Type BACKGROUND
PMID: 23945994 (View on PubMed)

Chipman JJ, Sanda MG, Dunn RL, Wei JT, Litwin MS, Crociani CM, Regan MM, Chang P; PROST-QA Consortium. Measuring and predicting prostate cancer related quality of life changes using EPIC for clinical practice. J Urol. 2014 Mar;191(3):638-45. doi: 10.1016/j.juro.2013.09.040. Epub 2013 Sep 25.

Reference Type BACKGROUND
PMID: 24076307 (View on PubMed)

Wagner AA, Cheng PJ, Carneiro A, Dovirak O, Khosla A, Taylor KN, Crociani CM, McAnally KC, Percy A, Dewey LE, Sanda MG, Chang P. Clinical Use of Expanded Prostate Cancer Index Composite for Clinical Practice to Assess Patient Reported Prostate Cancer Quality of Life Following Robot-Assisted Radical Prostatectomy. J Urol. 2017 Jan;197(1):109-114. doi: 10.1016/j.juro.2016.07.080. Epub 2016 Jul 27.

Reference Type BACKGROUND
PMID: 27475967 (View on PubMed)

Other Identifiers

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5108

Identifier Type: -

Identifier Source: org_study_id

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