A Study of Cognitive Health in Survivors of Prostate Cancer

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

ACTIVE_NOT_RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-09-08

Study Completion Date

2026-09-08

Brief Summary

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The purpose of this study is to collect information that may help the researchers understand the relationship between prostate cancer survivors' experiences of cancer-related cognitive dysfunction (CRCD) and their other conditions (co-morbid factors), including anxiety, depression, and insomnia. The researchers will also find out how additional things may contribute to CRCD, including social factors, the characteristics of participants' prostate cancer, and the type of cancer treatment or other medications they received.

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Detailed Description

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Conditions

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Prostate Cancer Survivorship

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Survivors of Prostate Cancer

This is a cross-sectional study with a one-time data collection process and no subsequent follow-ups. If patients did not opt out of receiving study-specific text communications, they may also receive text messages with reminders about surveys and/or direct links to REDCap to complete the surveys. Text-based communications will be delivered using the secure, HIPAA-compliant Mosio texting platform developed for clinical research.

PROMIS-SF v2.0 -Cognitive Function 8a

Intervention Type BEHAVIORAL

Patient-Reported Outcomes (PROs)

Interventions

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PROMIS-SF v2.0 -Cognitive Function 8a

Patient-Reported Outcomes (PROs)

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* English-speaking
* Age 18 years or older
* History of histologically documented PC of any stage
* No evidence of PC Disease

Exclusion Criteria

* \<1 month since completion of surgery, radiation, chemotherapy, or ADT
* Diagnosis of Alzheimer's disease, vascular dementia, Parkinson disease, or other organic brain disorder
* Score \>10 indicative of dementia on Blessed Orientation Memory Concentration

Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No