Actively Recruiting

Phase Not Applicable
Age: 25Years - 60Years
MALE
Healthy Volunteers
ID07195240

The Effect of Lemongrass on Aerobic Performance and Sexual Wellbeing Following High-Intensity Interval Training in Males

Led by Northumbria University · Updated on 2026-04-13

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

N

Northumbria University

Lead Sponsor

M

Mibelle Group Biochemistry

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the effects of lemongrass extract on aerobic training outcomes and sexual wellness in males aged 25 to 60 years. This randomized, double-blind, placebo-controlled trial aims to assess how a 6-week high-intensity interval training program combined with either lemongrass extract or a placebo affects aerobic capacity and sexual health. Participants will be randomly assigned to receive either 200 mg of lemongrass extract tablets or placebo tablets daily during the 6-week training. The training consists of three weekly sessions involving repeated high-intensity cycling intervals. The study includes multiple visits for familiarization, baseline testing, supervised training sessions, and post-intervention testing. Throughout the study, participants will undergo fitness tests, blood sampling, and complete questionnaires about sexual wellbeing. Key measures include aerobic capacity, blood lactate levels, heart rate, and serum analysis. After the final training session, participants will be followed up by phone to monitor any adverse effects, with total involvement spanning about eight weeks.

CONDITIONS

Brief Title

The Effect of Lemongrass on Aerobic Performance

Who Can Participate

Age: 25Years - 60Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age  40 and  60 years
  • Body Mass Index (BMI)  19 and  35 kg/m2
  • Willingness and ability to comply with the protocol in the opinion of the Investigator
  • Judged by the Investigator to be in good health as assessed by a health screening questionnaire
  • Currently identifies as the same biological sex as at birth
  • Physical activity status between sedentary to moderately trained (meeting WHO guidelines for adults)
  • Blood pressure < 140/90 mmHg
Not Eligible

You will not qualify if you...

  • History of heart disease
  • Any disease interfering with nutrient absorption (e.g., Crohn's disease, celiac disease)
  • Recent musculoskeletal or soft tissue injury within the last 3 months
  • Habitual use of antihypertensive or antidiabetic medication or medications affecting study participation
  • Alcohol intake greater than 21 units per week
  • Change in body weight of more than 3 kg in the month before the study
  • Currently following a weight-loss or weight-gain program
  • Known bleeding disorder or reaction to blood sample withdrawal

AI-Screening

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Your Study Journey

Screening

Duration - Up to 2 weeks

Participants are screened for eligibility to participate in the trial.

2 visits (pre-screening and familiarisation)

Baseline Assessment

Duration - 1 day

Participants complete baseline measurements including sexual wellbeing questionnaires, blood sampling, and exercise testing to determine aerobic capacity and performance.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants consume daily capsules of either lemongrass extract or placebo while completing high-intensity interval training sessions three times per week for six weeks.

18 training visits (3 visits per week)

Post-treatment Assessment

Duration - 1 day

Participants repeat baseline assessments including exercise testing, blood sampling, and questionnaires within 48 hours after the final training session.

1 visit (in-person)

Follow-up

Duration - Within 7 days after final visit

Participants receive a follow-up telephone call within 7 days to check for any adverse effects from participation.

1 telephone call

Trial Site Locations

Total: 1 location

1

Northumbria University

Newcastle upon Tyne, United Kingdom

Actively Recruiting

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Research Team

E

Emma Squires, Dr

G

Gill Drinkald

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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