The study will be a randomized clinical trial and will be conducted in Civil Hospital and Kalsoom Hospital Samundry. This study will be completed in time duration of 10 months after the approval of synopsis. Non probability convenience sampling with Randomization technique will be used and 26 participants will be recruited in study after randomization. The subjects will be divided into two groups and the group A will receive Progressive training and Health education and group B will receive only Health education. The data will be assessed at the baseline and after 8th week of treatment. After data collection data will be analyzed by using SPSS version 21.
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Hot Flash related Interference Scale (HFRDIS) for vasomotor symptoms
Timeframe: 6th week
FATIGUE SEVERITY SCALE
Timeframe: 6th week
DASS-21( Depression, Anxiety and stress scale 21-item
Timeframe: 6th Week