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The Power of 24-hour: Co-designing Intervention Components

NCT06269159 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 210

Last updated 2024-05-20

No results posted yet for this study

Summary

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

  • Overweight and Obesity

Interventions

OTHER

Concept mapping: brainstorm

Group health care providers: * Duration: 1.5 hour for HCP via zoom session * Brainstorm question: what would help your clients to change their sedentary behavior into more physical activity? Group adults with overweight and obesity * Duration: online survey (REDCAP) of approx. 10 minutes * Brainstorm question via an online survey. What would help you to change your sedentary behavior into more physical activity?

OTHER

Concept mapping: clustering and rating

The same participant of the brainstorm session are asked to join session 2 to complete the clustering and rating). All interested adults will get access to the online cluster and rate tool described below. * Duration: flexible use of the online tool (available for two weeks) * The clustering and rating of all needs mentioned in session 1 will be done online and individually via a web application. In this online tool, the final list of 'needs' generated in session 1 will be presented. * Individually sort the 'needs' into groups and give the group a theme. In addition, each need will be scored on effectiviness, feasibility, modifiability. Thhe participants have unlimited access for two weeks.

Sponsors & Collaborators

  • University Hospital, Ghent

    lead OTHER

Principal Investigators

  • Bruno Lapauw · University Hospital, Ghent

  • Marieke De Craemer · University Ghent

Eligibility

Min Age
25 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-05
Primary Completion
2025-03-31
Completion
2025-03-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06269159 on ClinicalTrials.gov