The Effect of Sensory Awareness Training Given to Women of Reproductive Age on Dysmenorrhea and Kinesiophobia
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: sensory awareness training.
- Who it may be relevant to
- Registry conditions: Dysmenorrhea, Kinesiophobia. Basic parameters: from 19 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This research investigates the use of web-based sensory awareness training given to women of reproductive age. It was planned to examine the effect of dysmenorrhea level and kinzeophobia status.H0a = Body weight of women of reproductive age who received and did not receive sensory awareness training. There is no difference between awareness levels. 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.
Detailed description
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. 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.
Interventions
- Behavioral 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.
Primary outcome measures
- Introductory Information Form [Time frame: Baseline]
- Tampa Kinesiophobia Scale [Time frame: day 1]
- Dysmenorrhea Affect Scale [Time frame: day 1]
- Multidimensional Body Awareness Assessment-II Scale [Time frame: day 1]
Secondary outcome measures (3)
- Tampa Kinesiophobia Scale [Time frame: up to 4 weeks]
- Dysmenorrhea Affect Scale [Time frame: up to 4 weeks]
- Multidimensional Body Awareness Assessment-II Scale [Time frame: up to 4 weeks]
Eligibility criteria
Inclusion criteria
- Volunteering to participate in research
- Having a complaint of dysmonea
- Being of childbearing age
- Being over 19 years old
- Having internet access
- Having a smart mobile phone
Exclusion criteria
- Be pregnant
- Having any disease that affects the menstrual period
- Using oral contraceptives
- Using intrauterine device
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Health services research
Study locations
Turkey (Türkiye) · 1 center
- Sağlık Bilimleri Üniversitesi — Istanbul
Identifiers
NCT: NCT07097285 · SBÜ-AYDINKARTAL-015