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Clinical Trials in Turkey / NCT07097181
Starting soon Not applicable

The Effect of Sensory Awareness Education on Female Students' Body Awareness and Premenstrual Symptom Levels

NCT07097181 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-08-31
Last updated
2025-07-31

Condition(s) studied

for GirlsSensory Awareness TrainingBody AwarenessPremenstrual SyndromeEffect

Investigational drug(s) / intervention(s)

web-based sensory awareness training

web-based sensory awareness training: The girl in the intervention group of the study 4 weeks to inform students, raise awareness and provide sensory education. Sensory awareness training will be provided throughout. Presentations to inform during training will be done, then Graded Sensory Discrimination, Graded Motor Imagery (DMI) and a home exercise program, as well as a body awareness training program. protocol will be applied.

Study summary

This research investigates the effects of web-based sensory awareness training on female students' body movements.

In order to examine its effect on awareness and premenstrual symptom levels. planned. H0a = Body awareness levels of female students who receive and do not receive sensory awareness training. There is no difference between.

H1a = Body awareness levels of female students who receive and do not receive sensory awareness training. There is a difference between .

H0b = Premenstrual symptoms of female students who received and did not receive sensory awareness training. There is no difference between the levels.

H1b = Premenstrual symptoms of female students who receive and do not receive sensory awareness training. There is a difference between the levels.

Participants will be given sensory awareness training for 4 weeks and female students will be given "Premenstrual Syndrome Scale" and "Very" before the training and 4 weeks after the first training.Dimensional Body Awareness Assessment-II Scale" will be applied

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Volunteering to participate in research. * University of Health Sciences, Hamidiye Faculty of Health Sciences, Department of Midwifery Being an active student in the first grade. * University of Health Sciences, Hamidiye Faculty of Health Sciences, Physiotherapy and Being an active female student in the first year of the Department of Rehabilitation. * Having internet access. * Having a smart mobile phone. Exclusion Criteria: * University of Health Sciences, Hamidiye Faculty of Health Sciences, Department of Midwifery Being a passive student in the first grade. * University of Health Sciences, Hamidiye Faculty of Health Sciences, Physiotherapy and Being a passive female student in the first year of the Rehabilitation Department.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sağlık Bilimleri Üniversitesi Istanbul Turkey (Türkiye)

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07097181 on ClinicalTrials.gov ↗ ← All trials in Turkey