Tokyo, Feb. 9 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000060617) titled 'Effects of a Health Fitness Programmer Led Multicomponent Exercise Intervention on Locomotive Syndrome in Community Dwelling Older Adults' on Feb. 8.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Open -but assessor(s) are blinded
Control - No treatment
Primary Sponsor:
Institute - Kameda Medical Center
Condition:
Condition - Locomotive syndrome
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - The objective of this study is to examine the effects of a Health Fitness Programmer led multicomponent exercise intervention on locomotive syndrome in community dwelling older adults using a randomized controlled trial design
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Participants in the locomotive training group will perform locomotive syndrome focused exercises, including exercises such as squats and single leg standing, under the supervision of a Health Fitness Programmer. The intervention will be conducted for 2 months, with a total of 24 sessions.
Interventions/Control_2 - Participants in the multicomponent exercise group will engage in a multicomponent exercise program targeting muscle strength, balance, flexibility, and walking ability under the supervision of a Health Fitness Programmer. The program will be conducted for 2 months, with a total of 24 sessions.
Eligibility:
Age-lower limit - 60
years-old
<=
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - Participants will be eligible if they meet all of the following criteria
1) Aged 60 years or older
2) No medical restriction on exercise as determined by a physician
3) Able to understand the study procedures and provide written informed consent
Key exclusion criteria - Participants will be excluded if they meet any of the following criteria
1) Cognitive impairment defined as a score of 20 or less on the Revised Hasegawa's Dementia Scale assessed within the past 3 months
2) Difficulty in attending the assessment and exercise sessions independently on foot (unable to ambulate independently to the venue)
Target Size - 68
Recruitment Status:
Recruitment status - No longer recruiting
Date of protocol fixation - 2025 Year 10 Month 02 Day
Date of IRB - 2025 Year 10 Month 02 Day
Anticipated trial start date - 2025 Year 10 Month 08 Day
Last follow-up date - 2026 Year 03 Month 30 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068785
Disclaimer: Curated by HT Syndication.