Tokyo, Aug. 7 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058711) titled 'Randomized Controlled Study of the Efficacy of Sweet-Salty Solution Discrimination Training' on Aug. 6.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Single blind -participants are blinded
Control - No treatment
Primary Sponsor:
Institute - Tohoku University
Condition:
Condition - healthy adult
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To investigate the effectiveness of sweet-salty mixture discrimination training using solutions containing sweet and salty tastes.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Sweet-salty mixture discrimination training
Interventions/Control_2 - Control group
Eligibility:
Age-lower limit - 20
years-old
Gender - Male and Female
Key inclusion criteria - Healthy adult men and women with no history of taste disorders and not currently diagnosed with any taste disorder or abnormality by a physician.
Individuals who have provided written informed consent to participate in the study.
Key exclusion criteria - Individuals deemed inappropriate for study participation by a physician
Individuals who declined to participate in the study
Individuals with known allergies to sucrose or sodium chloride
Smokers
Target Size - 38
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 07 Month 07 Day
Anticipated trial start date - 2025 Year 09 Month 01 Day
Last follow-up date - 2030 Year 08 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067122
Disclaimer: Curated by HT Syndication.
