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

S

Saglik Bilimleri Universitesi

Status

Not yet enrolling

Conditions

for Girls
Body Awareness
Effect
Premenstrual Syndrome
Sensory Awareness Training

Treatments

Behavioral: web-based sensory awareness training

Study type

Interventional

Funder types

Other

Identifiers

NCT07097181
SBU-AYDINKARTAL-014

Details and patient eligibility

About

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

Full description

The study will be conducted online via https://teams.microsoft.com/v2/. Female first-year students from the Midwifery Department and the Physiotherapy and Rehabilitation Department of SBÜ Hamidiye Faculty of Health Sciences who volunteer to participate will be assigned to the intervention group (n=90) and control group (n=90) using random numbers generated via https://www.randomizer.org/ by the researchers. All participants will complete an introductory information form.

Female students in the intervention group will receive sensory awareness training for four weeks. The training content will include presentations on the Sensory System, Proprioception and Kinesthesia, and Interoception. Following the presentations, a protocol focusing on body awareness will be implemented, including graded sensory discrimination, graded motor imagery (GMI), interoception awareness training, interoceptive awareness exercises, and home exercise programs. Each training session will be planned to last 60 minutes.

A pre-training briefing session will be held with the female students assigned to the intervention group who volunteer to participate. The "Premenstrual Syndrome Scale" and the "Multidimensional Assessment of Interoceptive Awareness-II Scale" will be administered to the students before the training and four weeks after the first session. Each training session will be conducted once a week and will be limited to 60 minutes. The study forms will be administered to participants in person.

Enrollment

180 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

180 participants in 2 patient groups

Standard of care (n:90)
No Intervention group
Description:
No educational intervention will be made to the students in the control group.
web-based sensory awareness training (n:90)
Experimental group
Description:
Female students in the intervention group will receive sensory awareness training for four weeks. The training content will include presentations on the Sensory System, Proprioception and Kinesthesia, and Interoception. Following these presentations, a protocol focusing on body awareness will be implemented. This protocol will consist of graded sensory discrimination, graded motor imagery (GMI), interoception awareness training, interoceptive awareness exercises, and a home exercise program. Each training session will be planned to last 60 minutes. A pre-training briefing session will be held with female students who volunteer to participate and are assigned to the intervention group.
Treatment:
Behavioral: web-based sensory awareness training

Trial contacts and locations

1

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Central trial contact

Büşra HIZLIOL, Arş. Gör.; Yasemin AYDIN KARTAL, Doç. Dr.

Data sourced from clinicaltrials.gov

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