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Effect of a Calisthenic Exercises on Premenstrual Symptoms

H

Halic University

Status

Completed

Conditions

Menstrual Pain

Treatments

Other: Calisthenic home exercise programs

Study type

Interventional

Funder types

Other

Identifiers

NCT06530368
28.07.2024-MÇ

Details and patient eligibility

About

The aim of this study is to examine the effects of an eight-week calisthenic home exercise program on premenstrual symptoms, pain and sleep quality in young women.

Full description

The study was conducted on 30 volunteers who met the inclusion criteria among female students studying at Haliç University Faculty of Health Sciences. The "Premenstrual Syndrome Scale (PMSS)" was used to assess the individuals' premenstrual symptoms; the "Visual Analog Scale (VAS)" was used to assess pain for each of the abdominal, lumbar and general body pain; and the "Pittsburgh Sleep Quality Index (PSQI)" was used to assess sleep quality. Then, the participants were randomly divided into two groups as "Group 1: Control group (n=15)" and "Group 2: - Calisthenic home exercise group (n=15)". Participants in the first group were not subjected to any intervention and were asked not to participate in any exercise program for eight weeks. Participants in the second group were informed about calisthenic home exercise programs face to face and were asked to perform these exercises as home exercises for eight weeks. At the end of the treatment process, participants' PMSS, VAS and PSQI scores were re-evaluated.Statistical analysis will be performed with SPSS 24.0 program. If the data is parametric, paired sample t-test will be used for within-group evaluation; independent sample t-test will be used for between-group evaluation. If the data is non-parametric, Wilson test will be used for within-group evaluation and Mann Whitney U test will be used for between-group evaluation.

Enrollment

30 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a woman between the ages of 18-25
  • Studying at Halic University Faculty of Health Sciences
  • Voluntarily participating in the study
  • Having a normal menstrual cycle
  • Not exercising
  • Having a score above the mild level on the Premenstrual Syndrome Scale

Exclusion criteria

  • Having a condition that prevents exercise
  • Pregnancy
  • Menopause
  • Having a gynecological disease (endometriosis, ovarian cyst, pelvic infection, myoma/uterine tumor, etc.)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Group 1: Control group
No Intervention group
Description:
Participants in the first group were not subjected to any intervention and were asked not to participate in any exercise program for eight weeks.
Group 2: Calisthenic home exercise group
Experimental group
Description:
Participants in the second group were informed about calisthenic home exercise programs face to face and were asked to perform these exercises as home exercises for eight weeks.
Treatment:
Other: Calisthenic home exercise programs

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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