Global Overweight and oBesE (GLOBE) Patient Registry, Development and Implementation of Disease-specific: Severity, Quality of Life and Cost Instruments.
Recruiting · NCT07229027 · Observational (researchers observe without assigning treatment) · Lead sponsor: Medialis Ltd.
View the official record on ClinicalTrials.gov →What this trial is about
We are conducting this study to develop a disease-specific instrument, a quality of life instrument and a comprehensive list of costs associated with overweight and obesity.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Patient group
- Patient is aged ≥18 years at the time of survey completion.
- Patient has a BMI over 25 (self-reported)
- Patient is willing to participate in all study activities.
- Patient is able to read, write, and converse in English.
- Healthcare professional participant must meet the following criteria for inclusion in the study:
- HCP is aged ≥18 years at the time of survey completion.
- HCP is suitably qualified and involved in the healthcare management of patients with a BMI over 25
- HCP is willing to participate in all study activities.
- HCP is able to read, write, and converse in English.
Exclusion criteria
- A participant who meets any of the following criteria will be excluded from the study:
- Participants do not have the cognitive capacity to provide informed consent.
- Participants with severe co-morbidity that might affect study participation.
Where it is running
1 location listed.
- Online recruitment - Milton Keynes, United Kingdom