Effect of oral contraceptive consumption timing on substrate metabolism, cognition, and exercise performance in females: a randomised controlled trial

Abstract

The pharmacokinetic profile of oral contraceptives (OCs) results in an acute, transient increase in circulating synthetic reproductive hormones. The aim of this study was to examine the effects of acute OC ingestion on cognitive function, substrate metabolism and exercise performance. Sixteen combined OC (30 micrograms ethinyl oestradiol and 150mg Levonorgestrel) users ingested either their OC or placebo (PLA) in a randomised, double-blind, crossover manner. After 60 minutes, participants completed tests of verbal memory and verbal fluency, followed by sub-maximal treadmill exercise for 6 minutes at 60% lactate threshold (LT) and 90% LT where respiratory exchange ratio (RER), carbohydrate oxidation, fat oxidation, heart rate (HR), rating of perceived exertion (RPE), felt arousal and feeling scale were recorded. Participants then completed an incremental ramp test to exhaustion to assess time to exhaustion (TTE) and peak oxygen uptake (VO2peak), before ingesting the pill corresponding to the condition, they were not in. RER, arousal and feeling scale were all significantly lower in the OC condition compared to PLA (all P < 0.05) with no difference in HR, carbohydrate oxidation, fat oxidation, RPE, TTE or VO2peak (all P > 0.05). Verbal fluency score was significantly higher in the OC condition compared to PLA (P < 0.05), with no differences between conditions for any aspect of verbal memory (all P < 0.05). Combined OC ingestion acutely affects substrate metabolism, affective responses to exercise and verbal fluency. The timing of OC ingestion should be considered in relation to aspects of physiological function.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

NCT06560944

Funding Statement

This project was supported by internal funding from the University of Lincoln.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethical approval was received from the University of Lincoln Research Ethics Committee (718)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

留言 (0)

沒有登入
gif