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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06427603
Other study ID # RD/2022/2.12
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2024
Est. completion date January 2025

Study information

Verified date May 2024
Source Hong Kong Metropolitan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intervention aiming to improve cardiometabolic health by reducing prolonged sitting


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date January 2025
Est. primary completion date October 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: 1. are community-dwelling older adults aged 65 years or above, 2. are smartphone users, 3. sit for >= 6 hours per day 4. are overweight Exclusion Criteria: 1. are unable to walk independently with/without walking aids due to a physical disability; 2. have health conditions that hinder the adherence to intervention

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
physical activity
workshops and mobile apps: break sedentary behavior by activity breaks

Locations

Country Name City State
Hong Kong School of Nursing and Health Studies, Hong Kong Metropolitan University Ho Man Tin

Sponsors (1)

Lead Sponsor Collaborator
Hong Kong Metropolitan University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intervention feasibility will be assessed using a scale "Feasibility, appropriateness, and acceptability of the intervention" T2: post-intervention (week 12)
Secondary Sedentary behavior will be assessed using an accelerometer T1: baseline (before the study begins)
Secondary Sedentary behavior will be assessed using an accelerometer T2: post-intervention (week 12)
Secondary Sarcopenia score ranged from 0 to 20 will be assessed using the Strength, Assistance with walking, Rise from a chair, Climb stairs and (Calf) Falls (SARC-Calf) T1: baseline (before the study begins)
Secondary Sarcopenia score ranged from 0 to 20 will be assessed using the Strength, Assistance with walking, Rise from a chair, Climb stairs and (Calf) Falls (SARC-Calf) T2: post-intervention (week 12)
Secondary Blood glucose will be assessed using a portable blood monitoring device T1: baseline (before the study begins)
Secondary Blood glucose will be assessed using a portable blood monitoring device T2: post-intervention (week 12)
Secondary Blood lipid will be assessed using a portable blood monitoring device T1: baseline (before the study begins)
Secondary Blood lipid will be assessed using a portable blood monitoring device T2: post-intervention (week 12)
Secondary Blood pressure will be assessed using a portable blood monitoring device T1: baseline (before the study begins)
Secondary Blood pressure will be assessed using a portable blood monitoring device T2: post-intervention (week 12)
Secondary Muscle strength (handgrip strength) will be assessed using a hand-held dynamometer T1: baseline (before the study begins)
Secondary Muscle strength (handgrip strength) will be assessed using a hand-held dynamometer T2: post-intervention (week 12)
Secondary Physical performance will be assessed using Time-Up-to-Go (TUG) T1: baseline (before the study begins)
Secondary Physical performance will be assessed using Time-Up-to-Go (TUG) T2: post-intervention (week 12)
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