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The investigators recruited participants, who were female with LUTS 50 participants for known group validity and 80 normal control females to evaluate for construct validity and test for reliability by statistical analysis.
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50 females with LUTS will completed the ICIQ-FLUTS and IPSS and then again at 2 weeks apart to test for convergent validity and test-retest validity.
The normal control group 80 women will completed ICIQ-FLUTS LF for test of construct validity.
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130 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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