Obesity, Overweight
Conditions
Brief summary
The purpose of this survey is to collect information for scientific research and to identify the impact of overweight and obesity on health-related quality of life.
Interventions
No treatment is given
Sponsors
Novo Nordisk A/S
Study design
Observational model
COHORT
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Informed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). 2. Male or female, age above or equal to 18 years at the time of signing informed consent. 3. Not currently pregnant 4. Does not participate in intense fitness or body building program 5. Weight loss not through illness or injury 6. Lives in South Korea, Australia, or India 7. BMI above or equal to 18 and associated weight class (Normal Weight or above) will be determined by a programmed calculation based on participant-reported height and weight.
Exclusion criteria
1. Previous participation in this study. Participation is defined as having given informed consent in this study 2. Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation 3. Does not meet inclusion criteria.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Score on IWQOL-Lite validated | At time of survey response (Day 1) | Calculated score. Likert scale; 1=Never True, 5=Always True |
Countries
United Arab Emirates
Outcome results
None listed