NCT06427603RecruitingNot Applicable
Sit Less and Move More: A Feasibility Study on Physical Active Break Intervention and Improving Cardiometabolic Health
Hong Kong Metropolitan University1 site in 1 country30 target enrollmentStarted: October 1, 2025Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Intervention feasibility
Study Overview
Brief Summary
Intervention aiming to improve cardiometabolic health and physical function by reducing prolonged sitting
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- None (Participant, Investigator)
Eligibility Criteria
- Ages
- 65 Years to — (Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •are community-dwelling older adults aged 65 years or above,
- •are smartphone users,
- •sit for >= 6 hours per day
- •are overweight
Exclusion Criteria
- •are unable to walk independently with/without walking aids due to a physical disability;
- •have health conditions that hinder the adherence to intervention
Arms & Interventions
activity group
Experimental
Intervention: physical activity (Behavioral)
Outcomes
Primary Outcomes
Intervention feasibility
Time Frame: T2: post-intervention (week 12)
will be assessed using a scale "Feasibility, appropriateness, and acceptability of the intervention"
Secondary Outcomes
- Physical activity(T2: post-intervention (week 12))
- Muscle strength (handgrip strength)(T2: post-intervention (week 12))
- Physical performance(T2: post-intervention (week 12))
- Sedentary behavior(T2: post-intervention (week 12))
- Sarcopenia score ranged from 0 to 20(T2: post-intervention (week 12))
- Blood glucose(T2: post-intervention (week 12))
- Blood pressure(T2: post-intervention (week 12))
- Sedentary behavior(T2: post-intervention (week 12))
- Sarcopenia score ranged from 0 to 20(T2: post-intervention (week 12))
- Blood glucose(T2: post-intervention (week 12))
- Blood pressure(T2: post-intervention (week 12))
- Muscle strength (handgrip strength)(T2: post-intervention (week 12))
- Physical performance(T2: post-intervention (week 12))
- physical function(T2: post-intervention (week 12))
- Standing(T2: post-intervention (week 12))
- Sedentary behavior(T1: baseline (before the study begins))
- Sarcopenia score ranged from 0 to 20(T1: baseline (before the study begins))
- Blood glucose(T1: baseline (before the study begins))
- Blood pressure(T1: baseline (before the study begins))
- Muscle strength (handgrip strength)(T1: baseline (before the study begins))
- Physical performance(T1: baseline (before the study begins))
- physical function(T1: baseline (before the study begins))
- Physical activity(T1: baseline (before the study begins))
- Standing(T1: baseline (before the study begins))
Investigators
Dr Bonny WONG Yee Man
Assistant Professor
Hong Kong Metropolitan University
Study Sites (1)
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