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Clinical Trials/NCT05243927
NCT05243927
Unknown
Not Applicable

Comparison of Aerobic Exercise and Spinal Stabilization Exercises in Women With Primary Dysmenorrhea

Ankara Yildirim Beyazıt University0 sites40 target enrollmentMarch 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Primary Dysmenorrhea
Sponsor
Ankara Yildirim Beyazıt University
Enrollment
40
Primary Endpoint
Menstrual pain intensity
Last Updated
4 years ago

Overview

Brief Summary

The aim of the study is to compare the effects of aerobic exercise and spinal stabilization exercises in women with primary dysmenorrhea (PD) complaints.

Detailed Description

PD is the cramping pain that comes before or during a period. Different exercise approaches have positive effects in PD. Comparing the effects of these exercise approaches is needed to determine the effects on PD.

Registry
clinicaltrials.gov
Start Date
March 2022
End Date
August 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Ankara Yildirim Beyazıt University
Responsible Party
Principal Investigator
Principal Investigator

seyda toprak celenay

associate professor

Ankara Yildirim Beyazıt University

Eligibility Criteria

Inclusion Criteria

  • Women with primary dysmenorrhea complaint according to the Primary Dysmenorrhea Consensus Guide, Over 18 years of age, Having a mean pain intensity of moderate and higher according to the Visual Analogue Scale in the last 6 months, Having a regular menstrual cycle (28±7 days), Volunteered to participate in the study.

Exclusion Criteria

  • Having a pathological history and radiological findings pointing to secondary dysmenorrhea, Using oral contraceptives/antidepressants at least 6 months, Receiving hormone therapy, Undergoing pelvic surgery, Pregnant, Giving birth, Using an intrauterine device, Having neurological, orthopedic and/or rheumatological diseases Having a history of ischemic heart disease (recently myocardial infarction, angina pectoralis, uncontrolled hypertension, etc.), Having a psychiatric disease, Having a history of malignancy

Outcomes

Primary Outcomes

Menstrual pain intensity

Time Frame: change from baseline at 8 weeks

Menstrual pain intensity will be evaluated with Visual Analogue Scale. This scale consists of a 10 cm horizontal line. The starting point "0" = "no pain", while "10" = "unbearable pain". Individuals will be asked to mark on a 10 cm straight line according to the level of pain they feel. Pain intensity will be recorded by measuring the distance between the beginning of the line and the marked place.

Secondary Outcomes

  • Impacts of life quality(change from baseline at 8 weeks)
  • Pelvic tilt(change from baseline at 8 weeks)
  • Functional capacity(change from baseline at 8 weeks)
  • Menstrual symptoms(change from baseline at 8 weeks)
  • Impacts of academic/work performance(change from baseline at 8 weeks)
  • Trunk muscle endurances(change from baseline at 8 weeks)
  • Functional and emotional effects(change from baseline at 8 weeks)
  • Sleep quality(change from baseline at 8 weeks)
  • Posture(change from baseline at 8 weeks)
  • Subjective perception of improvement(After exercise program (at 8 week))

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