DBPCT Effects of Omega-3 FA on Memory and Cognition in Peri- and Menopausal Women
NCT07814300, Not applicable, Active not recruiting, St. Mary's University, Twickenham
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | DBPCT Effects of Omega-3 FA on Memory and Cognition in Peri- and Menopausal Women | ClinicalTrials.gov |
| NCT number | NCT07814300 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 42 participants, actual | ClinicalTrials.gov |
| Lead sponsor | St. Mary's University, Twickenham | ClinicalTrials.gov |
| Conditions | Menopause | ClinicalTrials.gov |
| Interventions | A Randomised, Double-Blind, Placebo-Controlled Trial Investigating the Effects of Algae Omega-3 Fatty Acids on Memory and Cognition in Perimenopausal and Menopausal Women | ClinicalTrials.gov |
| First posted | 2026-09-10 | ClinicalTrials.gov |
| Last updated | 2026-09-10 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Verbal Memory | From baseline to completion, up to 31 days | Change in Memory scores from baseline to post-intervention, Rey Auditory Verbal Learning Test (RAVLT) | ClinicalTrials.gov |
| Primary | Working memory | From baseline to completion, up to 31 days | Change in memory from baseline to completion using the Digit Span Test | ClinicalTrials.gov |
| Primary | Verbal Adaptation | From baseline to completion, up to 31 days | Change in verbal adaptation from baseline to completion using the Stroop Test | ClinicalTrials.gov |
| Secondary | Change in menopausal symptoms (quality of life) | From baseline to completion, up to 31 days | Change in menopausal symptoms assessed using the Menopause-Specific Quality of Life (MENQOL) questionnaire. | ClinicalTrials.gov |
| Secondary | Change in subjective memory function | From baseline to completion, up to 31 days | Change in self-reported memory lapses measured using the Prospective and Retrospective Memory Questionnaire (PRMQ). | ClinicalTrials.gov |
| Secondary | Dietary patterns | From baseline to completion, up to 31 days | Dietary patterns assessed using a short Food Frequency Questionnaire to account for habitual nutrient intake that may influence outcomes. | ClinicalTrials.gov |
| Secondary | Sleep patterns | Baseline (Week 0; 7-day recording period prior to intervention)End of intervention (Week 12; 7-day recording period) | Change in sleep duration, sleep quality, and number of night-time awakenings, recorded using daily sleep diaries over 7 consecutive days. | ClinicalTrials.gov |
| Secondary | Stress levels | From baseline to completion, up to 31 days | Change in self-reported stress levels are integrated in self-reported questionnaire | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Digit Span Test | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Verbal Learning | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)