Trial · NCT02775084
Fish Oil T Cell Function
NCT02775084, Not applicable, Completed, Texas A&M University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Fish Oil T Cell Function. Trials, record NCT02775084. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02775084
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Fish Oil T Cell Function
- NCT number
- NCT02775084
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 13 participants, actual
- Lead sponsor
- Texas A&M University
- Conditions
- Muscle Strength, Cognitive Function
- Interventions
- Fish Oil, Olive Oil
- First posted
- 2016-05-17
- Last updated
- 2019-04-22
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in function of of lipid rafts in immune cell membranes due to dietary polyunsaturated fatty acids supplementation | one time on baseline, day 21 and day 42 | one blood draw on each study visit |
| Secondary | Fatty acid metabolism | one time on baseline, day 21 and day 42 | One blood draw on each study visit |
| Secondary | Skeletal muscle strength of hand | 30 minutes on baseline, day 21 and day 42 | Measurement of hand grip strength |
| Secondary | Skeletal muscle strength of leg | 30 minutes on baseline, day 21 and day 42 | Measurement of muscle strength of leg using kin-com machine |
| Secondary | Body Composition | 15 minutes on baseline, day 21 and day 42 | Body composition as measured by Dual-Energy X-ray Absorptiometry |
| Secondary | Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS | Postabsorptive state during 1 hours and change after feeding on baseline and change from day 21 and day 42 | A fourteen item self-assessment scale. Seven of the items related to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression. |
| Secondary | Diet recall | on baseline and change from day 21 and day 42 | The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day. |
| Secondary | Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT) | Postabsorptive state during 1 hours and change after feeding on baseline and change from day 21 and day 42 | A word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match. The examinee reads the words or names the ink colors as quickly as possible within a time limit. Measures selective attention and inhibitory control. The total time in seconds was reported for each trial. |
| Secondary | Group differences in attention and executive functions as measured by Trail Making Test (TMT) | Postabsorptive state during 1 hours and change after feeding on baseline and change from day 21 and day 42 | In Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy. In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy. Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility. The total time in seconds was reported for each measure. |
| Secondary | Group differences in learning and memory as measured by Digit Span | Postabsorptive state during 1 hours and change after feeding on baseline and change from day 21 and day 42 | Recall of numbers in the same order (Digit Forward) and in reverse order (Digit Backward). Measures auditory attention and verbal working memory. |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
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 | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Trail Making Test A | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02775084
GET https://conductscience.org/api/trials/v1/NCT02775084/registered