Status:

NOT_YET_RECRUITING

AMPER Proof of Concept Study

Lead Sponsor:

University of Strathclyde

Collaborating Sponsors:

NHS Greater Glasgow and Clyde

Conditions:

Alzheimer's Dementia (AD)

Eligibility:

All Genders

50+ years

Phase:

NA

Brief Summary

The AMPER (Agent-based Memory Prosthesis to Encourage Reminiscing) system has been built to help people with Alzheimer's disease by improving their memory recall and quality of life. Alzheimer's often...

Eligibility Criteria

Inclusion

  • \- Diagnosis of probable Alzheimer's disease of mild to moderate severity according to DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition) and NINCS-ADRAD (National Institute of Neurological and Communicative Disorders and Stroke-Alzheimer's Disease and Related Disorders Association) criteria.
  • Age 50 or older
  • Sensory (visual and auditory), language, and physical abilities adequate to perform assessments (corrective aids allowed).
  • ACE III score between 20 and 82 (inclusive) (or equivalent score on MMSE (between 14 and 24, based on Law et al., 20123 equivalence data) or MOCHA (between 14 and 24 (based on Pendleberry et al., 2011 equivalence data).
  • Having a caregiver or family member who can attend all visits, perform assessments, and supervise administration of study.

Exclusion

  • Medical records indicate AD patients with the visual variant or having colour vision deficits.
  • Medical records indicate a CT or MRI within 24 months prior to screening that indicates a diagnosis other than probable Alzheimer's disease.
  • Medical records indicate any significant neurological disease other than probable AD (e.g. Parkinson's disease, Huntington's disease, brain tumor, normal pressure hydrocephalus, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, history of stroke, or history of head injury requiring hospitalization).
  • On review of medical records, no clinically significant abnormal findings on previous physical examination, medical history, or clinical laboratory results that would indicate an alternative diagnosis.
  • Current history of major psychiatric disorder (e.g. Major depression) (as indicated on medical records)
  • History of substance misuse (as indicated on medical records).

Key Trial Info

Start Date :

April 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

February 28 2026

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06894953

Start Date

April 1 2025

End Date

February 28 2026

Last Update

March 25 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University of Strathclyde

Glasgow, United Kingdom