The Effect of Progressive Muscle Relaxation Exercises on Premenstrual Syndrome, Anxiety, and Tendency to Violence in Young Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-24
SponsorIstanbul Medipol University Hospital

About this trial

This study results will provide evidence on the effectiveness of Progressive Muscle Relaxation Exercises (PMRE) as a complementary method in improving Premenstrual Syndrome (PMS), an important women's health issue. Additionally, it will contribute to the literature by shedding light on irritability and anxiety, which are common side effects of PMS.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Female students studying at Istanbul Aydın University, Faculty of Health Sciences, Those who score 111 or above on the Premenstrual Syndrome Scale (PMSS), Female students aged 18-24 will be included in the study.

Disqualifiers

Non-Turkish speakers, Individuals who cannot communicate normally, Students who are unable to comply with the exercise program will be excluded from the study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Other intervention

    Relaxation Exercises (Progressive Muscle Relaxation Exercises): Progressive muscle relaxation exercises, one of the relaxation techniques, will be used in this study. Participants will be instructed to sit in a comfortable position on a chair during the exercises. Clear and precise instructions will be provided to ensure proper execution. The exercise program will be conducted for 8 weeks, 3 days a week, for 30 minutes, under the supervision of an expert physiotherapist.

Treatment groups

84 Participants
are divided into 2 treatment groups
Group A: Exercise groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Premenstrual Syndrome Scale

Premenstrual Syndrome Scale (PMSS): Developed by Gençdoğan in 2006, this scale consists of 44 items in a five-point Likert format, with response options scored from 1 to 5.

Time frame
evaluations will be conducted at the day 1 and after 8 weeks.
2

Violence Tendency Scale

Violence Tendency Scale (VTS): Developed by Göka, Bayat, and Türkçapar (1995) for the Ministry of National Education to assess violence tendencies in secondary school students, the scale was later redesigned and validated in the Prime Ministry Family Research Institution's 1998 study on violence in family and society.

Time frame
evaluations will be conducted at the day 1 and after 8 weeks.
3

Beck Anxiety Inventory

Beck Anxiety Inventory (BAI): Developed by Beck and colleagues in 1988, the Beck Anxiety Inventory (BAI) consists of 21 items and follows a Likert-type (0-3) self-report format (Beck, Brown, Epstein, \& Steer, 1988).

Time frame
evaluations will be conducted at the day 1 and after 8 weeks.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Istanbul Medipol University Hospital

Lead sponsor

Medipol University

Sponsor institution

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