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RAR-CLA and cognition

The effect of rumenic acid rich conjugated linoleic acid supplementation on cognitive functioning

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29637
Enrollment
52
Registered
2019-03-12
Start date
2019-09-02
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cognitive impairment

Interventions

Subjects will receive a daily dose of 3.5g rumenic acid divided over six capsules (intervention) or six placebo capsules (control).

Sponsors

Stepan Specialty Products B.V.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Aged =65 years • At risk of cognitive impairment/ memory complaints • Able to understand and perform the study procedures

Exclusion criteria

Exclusion criteria: • Body Mass Index (BMI) >35 kg/m2 • Current use of medication belonging to the “sartans” or “glitazones” • Current use of >500 mg/day of acetylsalicylic acid • Current use of medication that affects inflammation (anti-inflammatory medication) • Fish consumption of more than 1 serving per week • Current or recent (<1 month) use of fish oil supplements • Current or recent (<1 month) use of anti-inflammatory dietary supplements such as quercetin, curcumin, resveratrol, and/or other flavonoids • Diabetes mellitus • Having a disease which interferes with the effect of the RAR-CLA supplement and/or with the outcome measure (cognitive functioning) as judged by medical doctor • Swallowing problems • Current participation in other scientific research with the exception of EetMeetWeet!

Design outcomes

Primary

MeasureTime frame
Episodic memory as measured with the RAVLT

Secondary

MeasureTime frame
cognitive functioning (episodic and working memory, attention, executive functioning, and psychomotor speed) as measured with a battery of cognitive tests, the evaluation of rumenic acid supplementation on anxiety, depressive symptoms, quality of life (measured with questionnaires), and plasma fatty acid status (measured in blood)

Contacts

Public ContactOndine van de Rest

Wageningen University & Research

Ondine.vandeRest@wur.nl0317-485867

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)