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

NCT07097181 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2025-07-31

No results posted yet for this 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

Conditions

  • for Girls
  • Sensory Awareness Training
  • Body Awareness
  • Premenstrual Syndrome
  • Effect

Interventions

BEHAVIORAL

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.

Sponsors & Collaborators

  • Saglik Bilimleri Universitesi

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-08-31
Primary Completion
2025-09-30
Completion
2025-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07097181 on ClinicalTrials.gov