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NCT06260696 Clinical Trial

Assessing Health-Related Quality of Life and Willingness to Pay for Weight Management in Asia-Pacific by Gender

Obesity Clinical Trial

— ASPECT - APAC  

Official title:
Assessing Health-Related Quality of Life and Willingness to Pay for Weight Management in Asia-Pacific by Gender

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06260696
Other study ID # DAS-7626
Secondary ID U1111-1282-5512
Status Completed
Phase
First received
Last updated
Start date August 10, 2023
Est. completion date October 5, 2023

Study information
Verified date February 2024
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 3000
Est. completion date October 5, 2023
Est. primary completion date October 5, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No treatment is given
No treatment is given

Locations
Country Name City State
United Arab Emirates Novo Nordisk Investigational Site Dubai

Sponsors (1)
Lead Sponsor Collaborator
Novo Nordisk A/S

Country where clinical trial is conducted

United Arab Emirates, 

Outcome
Type Measure Description Time frame Safety issue
Primary Score on IWQOL-Lite validated Calculated score. Likert scale; 1=Never True, 5=Always True At time of survey response (Day 1)
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