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Older Adult clinical trials

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NCT ID: NCT04020692 Recruiting - Surgery Clinical Trials

Home Improvement Initiative of the TRaitement Optimisé Medicamenteux After Hospitalization

IATRO'MED
Start date: July 16, 2019
Phase: N/A
Study type: Interventional

The hypothesis is that the intervention of an operational clinical pharmacy team (EOPC), targeting both patients and hospital and health care professionals, allows: i) to initiate a therapeutic review during hospitalization, ii) to accompany the patients upon hospital discharge, iii) to maintain, in outpatient care, the drug treatments that have been optimized during hospitalization. The main objective of the study is to demonstrate that the intervention of an EOPC in surgical departments and then in outpatient care makes it possible to maintain, 45 days after the discharge of the patients aged 65 years and over, the chronic outpatient treatments revised and optimized during the hospital stay. The secondary objectives are to measure the impacts of EOPC's intervention on: - unexpected readmissions, emergency use, medical complications and adverse drug reactions; - patient and health professional satisfactions (community pharmacists and physicians); - the costs of drug treatments in ambulatory care.

NCT ID: NCT03487835 Completed - Older Adult Clinical Trials

Role of Kinesiology Tape in Older Adults

Start date: December 2015
Phase: N/A
Study type: Interventional

Aim: The present study aimed to investigate the role of Kinesiology ('Kinesio') tape in the physiological risk of falling in older adults. Methods: Twenty two older adults aged over 65 years and living in nursing homes. After assessment of demographic information, they were randomized into one of two groups [(Kinesio tape (n = 22) and control (n = 20)]. Kinesio tape was applied on the Kinesio tape group only and worn during a 2-week intervention period. Participants were evaluated with the Visual Analog Scale, Berg Balance Scale, Timed Up and Go Test, Mini-Mental State Examination, 30-Second Sit to Stand test and Functional Independent Measurement instrument at baseline, after 2 weeks of application and at 2-week follow-up.