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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
On this page
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual) for eligibility assessment
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
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
Actively Recruiting
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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