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NCT05625425 · ClinicalTrials.gov registry record · NA

Wayfinding Intervention and Long-Term Memory

A NA study of Mild Cognitive Impairment and Long-Term Memory Decline, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
200
Enrollment target
1
Study location

NCT05625425 is a NA study of Mild Cognitive Impairment and Long-Term Memory Decline that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 200 participants, below the 1,270-participant average among 205 other Mild Cognitive Impairment trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05625425, a NA study of Mild Cognitive Impairment and Long-Term Memory Decline, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

Therapeutic treatment is yet available for declining memory, which is an impairment affecting the quality of life for many older adults and patients with cognitive impairment. Cognitive training with an immersive video game promises to drive hippocampal-cortical plasticity and associated gains that can restore memory capability or provide therapeutic treatment for memory deficits.

Interventions

  • BEHAVIORAL LabyrinthVR software
  • BEHAVIORAL Placebo Games software
  • BEHAVIORAL Labyrinth Tablet software
  • BEHAVIORAL Labyrinth VR wireless

Study Locations (1)

California

  • UCSF Mission Bay - San Francisco

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2024-01-01
Est. Completion 2027-01-31
Phase NA

What the Registry Record Tells You About NCT05625425

The ClinicalTrials.gov registry entry for NCT05625425 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,270-participant average among 205 other Mild Cognitive Impairment trials with a reported enrollment target (84% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Mild Cognitive Impairment appearing as the primary indexed condition, and to 4 interventions - of which LabyrinthVR software is the first listed.

NCT05625425 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT05625425 about?

NCT05625425 is a clinical study titled "Wayfinding Intervention and Long-Term Memory". Therapeutic treatment is yet available for declining memory, which is an impairment affecting the quality of life for many older adults and patients with cognitive impairment. Cognitive training with an immersive video game promises to drive hippocampal-cortical plasticity and associated gains that ...

What is the current status of trial NCT05625425?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2024-01-01. Estimated completion is 2027-01-31.

What conditions does trial NCT05625425 study?

This clinical trial studies the following conditions: Mild Cognitive Impairment, Long-Term Memory Decline.

What interventions are being tested in trial NCT05625425?

The interventions under investigation include: LabyrinthVR software (BEHAVIORAL), Placebo Games software (BEHAVIORAL), Labyrinth Tablet software (BEHAVIORAL), Labyrinth VR wireless (BEHAVIORAL).

Who is sponsoring clinical trial NCT05625425?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05625425 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.