Pilot and Feasibility Studies | 2019

Effect of fish oil supplement administration method on tolerability and adherence: a randomized pilot clinical trial

 
 
 
 
 
 
 

Abstract


ObjectivesAnecdotally, several strategies have been suggested in order to improve tolerability of fish oil supplements, but there is little evidence supporting any of these strategies. The aim of this study was to determine if there is a difference among four methods of oral administration of fish oil supplementation in terms of tolerability and adherence.MethodsA randomized, prospective, open-label, four-arm pilot study was conducted on 60 healthy adult subjects randomized to different fish oil supplement administration methods with (1) milk, (2) food, (3) an empty stomach, and (4) frozen capsules prior to ingestion. Each subject was instructed to take two capsules three times daily for 30 consecutive days. Adherence was assessed by pill counts. Adverse effects were assessed by survey and patient exit interview.ResultsNo apparent differences were demonstrated among the four administration groups in terms of adherence, reasons for non-adherence, or self-reported adverse effects.ConclusionsMethod of administration did not affect rates of adherence or incidence of adverse effects in a small cohort of healthy adults taking fish oil supplement capsules for 30\u2009days.Trial registrationClinicalTrials.gov NCT01471366. Registered November 16, 2011.

Volume 5
Pages None
DOI 10.1186/s40814-018-0387-0
Language English
Journal Pilot and Feasibility Studies

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