The Effect of Sensory Awareness Training Given to Women of Reproductive Age on Dysmenorrhea and Kinesiophobia
NCT ID: NCT07097285
Last Updated: 2025-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
40 participants
INTERVENTIONAL
2025-12-01
2026-06-01
Brief Summary
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H1a = Body size of women of reproductive age who receive and do not receive sensory awareness training. There is a difference between awareness levels.
H0b = Dysmenorrhea of women of reproductive age who received or did not receive sensory awareness training. There is no difference between the levels.
H1b = Dysmenorrhea among women of reproductive age who received and did not receive sensory awareness training. There is a difference between the levels.
H0c = Kinesiophobia in women of childbearing age who received or did not receive sensory awareness training. There is no difference between the situations.
H1c = Kinesiophobia in women of reproductive age who receive and do not receive sensory awareness training. There is a difference between situations Sensory awareness training was given to women in the intervention group of the study for 4 weeks. will be given. Training contents, Sensory System Training Presentation, Proprioception and Kinesthesia Sensory Training Presentation, Interoception Sense Training Presentation will be given, then Graded Sensory Discrimination, Graded Motor Imagery (DMI), interoception awareness training, body training with training consisting of interoceptive awareness exercises and home exercise programs. A protocol for awareness training will be implemented.
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Detailed Description
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A protocol for awareness training will be implemented. Each training is 60 minutes long will be planned. Women who volunteered to participate in the study and were assigned to the intervention group An informational meeting will be held before the training. 4 weeks from pre-training and first training "Tampa Kinesiophobia Scale (TKÖ)" "Dysmenorrhea Affectedness Scale" and "Very Dimensional Body Awareness Assessment-II Scale" will be applied. be once a week Each training period is limited to 60 minutes. Research forms were given to participants face to face. will be implemented.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Standard of care (n:40)
No intervention will be made to the control group.
No interventions assigned to this group
sensory awareness training (n:40)
Sensory awareness training was given to women in the intervention group of the study for 4 weeks. will be given. Each training is 60 minutes long will be planned. 4 weeks from pre-training and first training "Tampa Kinesiophobia Scale (TKÖ)" "Dysmenorrhea Affectedness Scale" and "Very Dimensional Body Awareness Assessment-II Scale" will be applied. be once a week Each training period is limited to 60 minutes. Research forms were given to participants face to face. will be implemented.
sensory awareness training
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. Graded Sensory Discrimination protocol, localization training It includes level 1, localization training level 2 and graphesthesia training. Graded Engine Visualization (DMI) protocol includes right/left discrimination training and visual imagery training.
Interventions
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sensory awareness training
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. Graded Sensory Discrimination protocol, localization training It includes level 1, localization training level 2 and graphesthesia training. Graded Engine Visualization (DMI) protocol includes right/left discrimination training and visual imagery training.
Eligibility Criteria
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Inclusion Criteria
* Having a complaint of dysmonea
* Being of childbearing age
* Being over 19 years old
* Having internet access
* Having a smart mobile phone
Exclusion Criteria
* Having any disease that affects the menstrual period
* Using oral contraceptives
* Using intrauterine device
19 Years
FEMALE
No
Sponsors
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Saglik Bilimleri Universitesi
OTHER
Responsible Party
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YASEMİN AYDIN KARTAL
Doç. Dr.
Locations
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Sağlık Bilimleri Üniversitesi
Istanbul, , Turkey (Türkiye)
Countries
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Central Contacts
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Other Identifiers
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SBÜ-AYDINKARTAL-015
Identifier Type: -
Identifier Source: org_study_id
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