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Clinical Trials/NCT06208475
NCT06208475CompletedNot Applicable

The Effects of Resistance Exercise on Appetite Control, Food Reward, and Energy Intake in Different Menstrual Cycles

National Taiwan Normal University1 site in 1 country18 target enrollmentStarted: August 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
18
Locations
1
Primary Endpoint
Change in total-GLP-1

Study Overview

Brief Summary

The study aims to provide insights into how menstrual cycle phases impact appetite responses to resistance exercise in young women. Healthy young women will participate in four trials: the exercise session in the follicular phase, the exercise session in the luteal phase, the control session in the follicular phase, and the control session in the luteal phase. Various measurements will be taken, including subjective appetite perceptions, appetite hormones, food preferences, lactate levels, estradiol levels, progesterone levels, and energy intake.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 30 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Age: 20-30
  • •Healthy female with normal menstruation
  • •Weight stable for at least 6 months

Exclusion Criteria

  • •Overweight (BMI > 30 kg/m^2 or body fat > 30%)
  • •Hypertension (> 140/90 mmHg)
  • •Cardiovascular disease, cancer or other chronic diseases

Arms & Interventions

The exercise in the follicular phase (EF)

Experimental

Resistance exercise during the early-follicular phase (approximately during days 1-7 of the menstrual cycle).

Intervention: Resistance exercise (Other)

The exercise in the luteal phase (EL)

Experimental

Resistance exercise during the mid-luteal phase (approximately during days 18-25 of the menstrual cycle).

Intervention: Resistance exercise (Other)

The control in the follicular phase (CF)

No Intervention

Sit and rest during the early-follicular phase (approximately during days 1-7 of the menstrual cycle).

The control in the luteal phase (CL)

No Intervention

Sit and rest during the mid-luteal phase (approximately during days 18-25 of the menstrual cycle).

Outcomes

Primary Outcomes

Change in total-GLP-1

Time Frame: 4 hours during each study intervention

total-GLP-1 in pg/mL

Change in active-GLP-1

Time Frame: 4 hours during each study intervention

active-GLP-1 in pg/mL

Change in total-Ghrelin

Time Frame: 4 hours during each study intervention

total-Ghrelin in pg/mL

Change in acyl-Ghrelin

Time Frame: 4 hours during each study intervention

acyl-Ghrelin in pg/mL

Change in PYY

Time Frame: 4 hours during each study intervention

PYY in pg/mL

Change in lactate

Time Frame: 4 hours during each study intervention

insulin in mmol/L

Subjective appetite

Time Frame: 4 hours during each study intervention

The appetite perceptions are obtained through a 0-100 mm visual analog scale. The variables assessed include perceptions of hunger (i.e., "How hungry do you feel?"), satisfaction (i.e., "How satisfied do you feel?"), fullness (i.e., "How full do you feel?"), prospective food consumption (i.e., "How much do you think you can eat?"), and nausea (i.e., "How nauseous do you feel?"), with 0 indicating "not at all" and 100 signifying "extremely.".

Secondary Outcomes

  • Explicit liking(4 hours during each study intervention)
  • Implicit wanting(4 hours during each study intervention)
  • Taste appeal bias(4 hours during each study intervention)
  • Change in glucose(4 hours during each study intervention)
  • Explicit wanting(4 hours during each study intervention)
  • Relative preference(4 hours during each study intervention)
  • Fat appeal bias(4 hours during each study intervention)
  • Energy intake(3 days during each study intervention)
  • Change in TG(4 hours during each study intervention)
  • Change in insulin(4 hours during each study intervention)
  • Sex hormones(4 hours during each study intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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