Actively Recruiting
The Power of 24-hour: Co-designing Intervention Components
Led by University Hospital, Ghent · Updated on 2024-05-20
210
Participants Needed
1
Research Sites
81 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Most of the existing lifestyle interventions in adults with overweight or obesity focus on one movement behavior in isolation (i.e. moderate to vigorous physical activity (MVPA)). However, recent research suggests to incorporate all movement behaviors performed in one day to explore the possible synergistic health effects of targeting more than one behavior. Moreover, more optimal 24-hour movement behavior compositions are related with better cardiometabolic health. Literature shows that adults with obesity have less optimal 24-hour compositions (8-9). Therefore it would be of interest to discover the needs related to an optimal 24-hour movement behavior intervention for a group of adults with overweight and obesity using co-design to develop an intervention. This study will conduct a concept mapping protocol to explore the needs to of people with overweight and obesity to change their sedentary behavior into more physical activity as well to include the opinion of health care providers (HCP are physiotherapists) on the needs of their patients.
CONDITIONS
Official Title
The Power of 24-hour: Co-designing Intervention Components
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 25 to 64 years
- Currently working at least 50 percent of a full-time job
- Body mass index (BMI) of 25 kg/m² or higher
- Healthcare providers included are physiotherapists and movement on referral coaches working with clients on healthy lifestyle and overweight or obesity
You will not qualify if you...
- Retirement or early retirement
- Unemployed status
- Working less than 50 percent
- Working night shifts
- Physical conditions like amputations, paralysis, stroke recovery, osteoarthritis
- Cognitive conditions such as dementia or psychological disorders
- Major medical conditions including chronic respiratory diseases, heart failure, cardiovascular diseases, cancer
- Diabetes diagnosed by a general practitioner
- Currently pregnant or pregnancy within the past year
- Participation in study-specific weight loss interventions
- Post-surgery weight loss interventions
- On waitlist for weight loss surgery
- Currently hospitalized
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ghent university Hospital
Ghent, Belgium, 9000
Actively Recruiting
Research Team
I
Iris Willems
CONTACT
M
Marieke De Craemer
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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