Alzheimer's Disease Trial, Recruiting NCT02434393 Sponsor: University of Southern California Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT02434393
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who previously took part in either the "Characterizing Cognitive Decline in Late Life Depression" study or the "Multimodal MRI Characteristics of Psychotherapy Response in Late Life Depression" study.
  • People currently taking antidepressant medication, as long as the dose has stayed the same for at least 4 weeks before the MRI scan.
  • People currently receiving psychotherapy (individual or group talking therapy), as long as at least 4 weeks of that therapy have been completed before the MRI scan.
  • People taking medications that are intended to support memory or thinking (sometimes called cognitive enhancing medications).

Who may not be able to join:

  • No specific exclusion criteria were listed in the official criteria provided (confirm with trial site).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Scott Mackin, PhD, University of California, San Francisco

Phone: (415) 300-0582

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
4 March 2015
Est. completion
1 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Rate of Change in neuropsychological measures of executive function as measured by the Digit Symbol Substitution Test using total correct.; Rate of Change in expressive language as measured by the Boston Naming Test using total correct.; Rate of change in learning and memory as measured by the Rey Auditory Verbal Learning Test using total correct and delayed recall.; Change in brain structure using magnetic resonance imaging (MRI); Extent of amyloid deposition as measured by florbetapir; Extent of tau deposition as measured by flortaucipr

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov