Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
ID07391930

Efficacy of a High-Intensity Interval Training Program and Analysis of Menstrual Health Experience in Women With Primary Dysmenorrhea: A Mixed-Methods Randomized Controlled Trial.

Led by University of Alcala · Updated on 2026-04-21

60

Participants Needed

1

Research Sites

52 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are evaluating whether a 12-week online supervised high-intensity interval training (HIIT) program can reduce menstrual pain and improve quality of life in women aged 18 to 40 with primary dysmenorrhea. The study also explores how this exercise affects women's personal experiences with their bodies and menstruation, aiming to provide new non-drug methods for managing menstrual pain through both a randomized controlled trial and qualitative analysis. Participants are divided into two groups: one group receives a 2-hour online menstrual health education workshop plus twice-weekly supervised online HIIT sessions for 12 weeks, while the control group receives only the educational workshop. All participants complete weekly digital diaries during the intervention. Clinical measures such as pain intensity, quality of life, sleep quality, mood, and work productivity are collected at baseline, immediately after the intervention, and at follow-up visits up to nine months. During the study, participants will be assessed using pain scales, questionnaires, and weekly diary entries to capture both physical symptoms and personal menstrual health experiences. Researchers will analyze changes in pain intensity and other health outcomes over time, integrating quantitative results with diary insights to understand biopsychosocial effects. The total participation includes the initial 12-week intervention and follow-up assessments through month nine, with safety and adherence monitored throughout.

CONDITIONS

Brief Title

High-Intensity Interval Training and Menstrual Health Experience in Primary Dysmenorrhea.

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female, aged 18 to 40 years
  • Nulliparous women with primary dysmenorrhea
  • Body mass index between 18 and 30
  • Menstrual pain greater than 5 on the Numeric Pain Scale
  • Currently exercising more than 45 minutes per week
  • Able to understand Spanish and provide informed consent
Not Eligible

You will not qualify if you...

  • Having amenorrhea or menstrual cycles longer than 35 days
  • Secondary dysmenorrhea (menstrual pain caused by other conditions)
  • Previous pelvic or abdominal surgery
  • Use of hormonal drugs
  • Diagnosed with fibromyalgia, musculoskeletal injuries, or other medical conditions preventing intense exercise
  • Currently receiving physiotherapy for pelvic floor disorders
  • Exercising more than 75 minutes per week

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual) for eligibility assessment

Treatment

Duration - 12 weeks

Participants receive a 2-hour online menstrual health education workshop. Those in the experimental group also participate in 24 supervised online high-intensity interval training (HIIT) sessions over 12 weeks (2 sessions per week). All participants complete weekly qualitative diaries during this period.

1 educational workshop and twice-weekly supervised online exercise sessions for 12 weeks; weekly diary entries

Follow-up

Duration - 3 months

Participants complete follow-up assessments to evaluate changes in menstrual pain intensity, quality of life, sleep quality, mental health, and work productivity after the intervention period.

Assessments at 3 months post-intervention and again at 6 months post-intervention

Trial Site Locations

Total: 1 location

1

Universidad de Alcalá, Facultad de Enfermeria y Fisioterapia

Alcalá de Henares, Madrid, Spain, 28801

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Research Team

E

Esther M Pindado Perez, PhD Student

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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