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The Effects Of Relaxation Training In Women With Primary Dysmenorrhea

Not Applicable
Conditions
Primary Dysmenorrhea
Interventions
Other: No intervention
Other: Relaxation training
Registration Number
NCT05328869
Lead Sponsor
Ankara Yildirim Beyazıt University
Brief Summary

The aim of this study was to investigate the effects of relaxation training on menstrual pain severity, menstrual symptoms, impact of quality of life, impact of work/academic performance, impact of social activity level and anxiety level in women with primary dysmenorrhea (PD) complaints.

Detailed Description

PD is the cramping pain that comes before or during a menstrual period. Relaxation training contributes to the reduction of stress and pain. Thus, there is a need to investigate the effects of relaxation training in dysmenorrhea.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
30
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 psychiatric disease,
  • Having a history of malignancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupNo interventionNo intervention will be applied
Relaxation groupRelaxation trainingJacobson progressive relaxation training will be applied
Primary Outcome Measures
NameTimeMethod
Menstrual pain intensitychange from baseline at an average of 2 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 Outcome Measures
NameTimeMethod
Impacts of social activitychange from baseline at an average of 2 weeks

Impacts of social activity will be evaluated with Visual Analogue Scale. This scale consists of a 10 cm horizontal line. The starting point "0" = "my social activity is not affected in any way", while "10" = "my social activity is greatly affected". Individuals will be asked to mark on a 10 cm straight line according to the social activity they think.

Anxiety levelchange from baseline at an average of 2 weeks

Anxiety level will be assessed with the Spielberger State Trait Anxiety Inventory. This inventory is a 40-item self-report inventory designed to measure both state anxiety section (current feelings of apprehension, worry, etc.) and trait anxiety section (continuous feelings of apprehension, worry, etc.). Each section is scored on four levels of anxiety intensity from 1="not at all" to 4="very much" and with a sum score between 20 and 80. A higher total score indicates more severe anxiety level.

Impacts of life qualitychange from baseline at an average of 2 weeks

Impacts of life quality will be evaluated with Visual Analogue Scale. This scale consists of a 10 cm horizontal line. The starting point "0" = "my quality of life is not affected in any way", while "10" = "my quality of life is greatly affected". Individuals will be asked to mark on a 10 cm straight line according to the quality of life they think.

Menstrual symptomschange from baseline at an average of 2 weeks

Menstrual symptoms will be measured with the menstrual symptom questionnaire. Menstrual Symptom Questionnaire is a 24-item self-report scale and each item is scored between 1 (never) and 5 (always). An increase in the mean score indicates an increase in the severity of menstrual symptoms. The total score is 120 points.

Impacts of academic/work performancechange from baseline at an average of 2 weeks

Impacts of academic/work performance will be evaluated with Visual Analogue Scale. This scale consists of a 10 cm horizontal line. The starting point "0"= means "my work/school performance is not affected in any way", while "10"= means "my work/school performance is greatly affected"

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