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The Effectiveness of an Intervention of Fresh Strawberries on Menstrual Pain and Menstrual Distress

NCT06250660 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2024-08-01

No results posted yet for this study

Summary

The purpose of this project is to know the effectiveness of an intervention based on the consumption of fresh strawberries from the Huelva region on menstrual pain and menstrual distress in young university students with primary dysmenorrhea, compared to a control group of students.

The participants with dysmenorrhea will be divided into two groups, the assignment will be random to the intervention group with strawberry intake for a month and comparing its effect with de control group. The results of the evaluations carried out prior, to the month and 2 months of the intervention will be compared.

Conditions

  • Primary Dysmenorrhea
  • Menstrual Pain
  • Menstrual Distress \(Dysmenorrhea\)

Interventions

DIETARY_SUPPLEMENT

Strawberry Intervention

This is an intervention based on the intake of strawberry, specifically the "Fortuna" variety. This intervention is based on the intake of 250 g of fresh strawberries per day for a month. The amount and duration of strawberry intake has been consulted in other studies carried out with strawberries.

Sponsors & Collaborators

  • University of Huelva

    collaborator OTHER

  • Cynthia del Rocío Márquez Beltrán

    lead OTHER

Principal Investigators

  • Elia Fernández Martínez, PHD · Teacher and Researcher

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-04-02
Primary Completion
2024-06-06
Completion
2024-06-06

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06250660 on ClinicalTrials.gov