NCT00579072Active, not recruiting
The Impact of Androgen Ablation Therapy on Cognitive Functioning and Functional Status in Men With Prostate Cancer Age 65 and Older
Source: ClinicalTrials.gov · Last updated 6 May 2026
Brief summary (registry, in English)
The purpose of this study is to find out if therapy with hormones (such as Lupron, Casodex, Zolodex or Degarelix) change a person's thinking abilities.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 230 (actual)
- First submitted
- 19 Dec 2007
- Start date
- Aug 2006
- Primary completion date
- Dec 2027
- Lead sponsor
- Memorial Sloan Kettering Cancer Center
- Diseases
- Prostate cancer
- NCT number
- NCT00579072
What you commit to
- Study type: Observational
- Participants enrolled: 230
- From Aug 2006 to the primary completion date, Dec 2027
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous or current treatment with chemotherapy
- Renal Transplant Clips
- Hearing Aids /implant
- Ocular Implants
- Hair implants
Other illness
- As per medical record or self-report, a history of central nervous system stroke, history of traumatic brain injury, or diagnosis of neurogenerative disorder that affects cognitive function (e.g. Alzheimer's, Parkinson's, Multiple Sclerosis, dementia, seizure disorders, etc.)
- History of untreated psychiatric disease
- As per medical record or self-report, history of loss of consciousness for 60+ minutes and/or admitted to the hospital for a head injury
- History of developmental disorders
- Current or history of alcohol or substance abuse
- Visual, auditory, or other impairment that would preclude ability to complete neuropsychological testing (e.g. significant macular degeneration, being unable to correct hearing with hearing aides, hand tremors, etc.)
- CRITERIA FOR OPTIONAL fMRI
- Cardiac pacemaker
- Artificial heart valve
Other
- All Groups
- Current use of opioids
- Patient has a self-reported fear of enclosed spaces (Claustrophobia)
- As per self report or as identified in the medical record, patient has any of the following items that preclude fMRI evaluation:
- Joint replacements
- Aneurysm clips
- Transdermal patched
- Aortic clips
- Prosthesis
- Intracranial bypass clips
- Harrington rod
- Coronary Artery bypass clips
- Biostimulator
- Bone or joint pins
- Other vascular clips or filters
- Tissue expander
- Implanted neurostimulators
- Metal mesh
- Stents
- Insulin pump
- Wire structures
- Electrodes
- Shrapnel/bullets
- Implanted electrical devices
- IUD Metal in eyes
- Shunts
- Hair extensions
- Tattoos above the waist
- Any possible metal in body
- As per self report, patient has dentures, body jewelry or wig that they are unable to remove
Who the study is looking for
- Comparison Androgen Ablation Group
- Diagnosis of prostate cancer
- Age 65 or older
- Ability to converse, write and read English
- In the investigator's judgment, participants must have satisfactory cognitive function to provide valid informed consent and participate in the neurocognitive testing. The Blessed Orientation-Memory-Concentration test (BOMC) will be used as a cognitive screening tool. Patients must have a BOMC score of less than or equal to 11.
- Able to provide informed consent
- Have been on continuous androgen ablation therapy for 6 months to-3 years
- Longitudinal Androgen Ablation Subgroup
- Diagnosis of prostate cancer
- Age 65 or older
- Ability to converse, write and read English
- Able to provide informed consent
- In the investigator's judgment, participants must have satisfactory cognitive function to provide valid informed consent and participate in the neurocognitive testing. The Blessed Orientation-Memory-Concentration test (BOMC) will be used as a cognitive screening tool. Patients must have a BOMC score of less than or equal to 11.
- Starting androgen ablation therapy or started within the past 21 days
- No androgen ablation therapy within the past year
- No Androgen Ablation Subgroup
- Diagnosis of prostate cancer
- Age 65 or older
- In the investigator's judgment, participants must have satisfactory cognitive function to provide valid informed consent and participate in the neurocognitive testing. The Blessed Orientation-Memory-Concentration test (BOMC) will be used as a cognitive screening tool. Patients must have a BOMC score of less than or equal to 11.
- At least 1-year post definitive localized treatment
- Ability to converse, write and read English
- Able to provide informed consent
- Not anticipated to start androgen ablation therapy
- No history of androgen ablation therapy
Age in the registry: 65 years to - · Sex: Male · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| City of Hope Coordinator of this site? Confirm its status | Duarte | United States | Unknown status |
| Memorial Sloan-Kettering Cancer Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.