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Completed

NCT Number: NCT00437983

The Efficacy of Phosphatidylserine-Omega3 in Elderly With Age Associated Memory Impairment

The primary objective of this trial is to assess the ability of an oral administration of Phosphatidylserine-Omega3 to improve attention and memory complaints in comparison to placebo in age associated memory impaired subjects.

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Key information

Age range

50 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

The Tel Aviv Sourasky Medical Center, Neurology department

Tel Aviv, 64239, Israel

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to give written informed consent
  • Age: 90≥ years ≥50
  • Gender: male and female
  • CDR ≤ 0.5
  • Complaints of memory loss reflected in such everyday problems as difficulty remembering names of individuals following introduction, misplacing objects, difficulty remembering multiple items to be purchased or multiple tasks to be performed, difficulty remembering telephone numbers or zip codes, and difficulty recalling information quickly or following distraction. Onset of memory loss must be described as gradual, without sudden worsening in recent months. Complaints of memory loss to be assessed by the MAC-Q scale.
  • Mini-Mental State Examination (MMSE) ≥27 for subjects with college education (BA) and ≥ 26 for all others
  • Memory test performance that is at least 1 SD below the mean established for young adults on at least one neuropsychological subtest of NexAde.
  • Language: Subjects must be able to read, write and speak Hebrew.
  • Ability to perform tests and interviews

Exclusion criteria

  • Evidence of delirium, confusion, or other disturbances of consciousness
  • Any Neurological disorder that could produce cognitive deterioration. Such disorders include AD, Parkinson's disease, stroke, intracranial hemorrhage, local brain lesions including tumors, and normal pressure hydrocephalus
  • History of any infective or inflammatory brain disease including those of viral, fungal, or syphilitic etiologies
  • Evidence of significant cerebral vascular pathology
  • Head injury immediately preceding cognitive deterioration.
  • Current psychiatric diagnosis according to DSM IV criteria of depression, mania, or any other major psychiatric disorder
  • Current diagnosis or history of alcoholism or drug dependence.
  • Evidence of depression as determined by the Geriatric Depression Scale (short version) score of 5 or more.
  • Any medical disorder that could produce cognitive deterioration including renal, respiratory, cardiac, and hepatic disease, diabetes mellitus, endocrine, metabolic or hematological disturbances unless well controlled, and malignancy not in remission for more than two years
  • Use of psychotropic drug or any other drug or supplement that may significantly affect cognitive functioning during the month prior to psychometric testing.
  • Use of any experimental medication within 1 month prior to screening or as concomitant medications.
  • Subject has a history of hypersensitivity or allergy to fish or fish oil or soy.

Treatment and study plan

PS-Omega3

Dietary Supplement

Phosphatidylserine-Omega3 capsules 3x100mg/day 15 wk. Next, follow up phase, open label,1x100mg/day, 15 wk

Placebo

Dietary Supplement

Placebo cellulose tainted with fishy odor capsules 3x100mg/day 15 wk

Primary outcomes

  1. Change From Baseline in Rey Auditory Verbal Learning Test

    Time frame: baseline, 15 wk

    A widely used, brief, easy to understand scale to evaluate verbal learning and memory. The score is presented as the number of words correctly recalled (0 is worse, 15 is best).The total learning task score ranges from 0 to 45 words(0 is worse, 45 is best).

Secondary outcomes

  1. Blood Work

    Time frame: baseline,15 wk

  2. Trail Making Test

    Time frame: Baseline, 15 weeks

  3. Computerized Cognitive Assessment Tool

    Time frame: baseline, 15 weeks

  4. Clinical Global Impression of Change (CGI-C)Scale

    Time frame: 7 weeks, 15 weeks

    The Clinical Global Impression of Change (CGI-C)scale is designed to record the clinician's global impression of change. Global improvement score ranges from 1 = "Very much improved", through 4 = "No change", to 7 = "Very much worse". Participants who experienced an improvement (scores 1, 2 or 3) in at least one of the two visits (following 7 or 15 weeks of treatment) were classified as improved over the treatment period (with the exception of participants reporting improvement following 7 weeks and deterioration at endpoint, who were NOT rated as improved)

  5. Change From Baseline in Rey Osterrieth Complex Figure Test

    Time frame: baseline, 15 weeks

    A widely used neuropsychological tool for the evaluation of visuospatial constructional ability and visual memory. Both the time to complete the task (copy time)and the accuracy (immediate and delayed recall) were used as measures for the analysis. Accuracy range score is 0-36 points (0 is worse, 36 is best). Copy time is expressed in seconds (less time to copy indicates better performance).

Sponsors and collaborators

Lead sponsor

Enzymotec

Industry

Registry information

Official study title

A Single-Center, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy of Phosphatidylserine-Omega3 in Elderly With Age Associated Memory Impairment

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Feb 21, 2007
Registry last updated
Jan 5, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.