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Persons With Obesity (PwO) Exploratory Research

Persons With Obesity (PwO) Exploratory Research - India

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05736120
Enrollment
46
Registered
2023-02-21
Start date
2023-02-19
Completion date
2023-04-19
Last updated
2023-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

The purpose of this study is to understand the personal flow along the weight loss management journey. A range of variables will be addressed in a survey to explore the weight loss journey, barriers and management. Topics include weight loss strategies and challenges, HCP involvement, and perceptions towards weight loss medications. Potential participants will be recruited using various online panels. Study participants will be recruited to participate in 2 types of qualitative research. Phase I: Online bulletin boards (OBB) Phase II: Virtual focus groups (real-time)

Interventions

OTHERNo treatment given

No treatment given

Sponsors

Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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. Current body mass index (BMI) of 25 or greater 4. Not currently pregnant 5. Does not participate in intense fitness or body building program 6. Weight loss not through illness or injury 7. At least somewhat concerned about current weight 8. If no plans for weight loss in the next six months, has made at least 1 weight loss effort in last 5 years 9. Struggling with weight for at least 3 years

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

MeasureTime frameDescription
Description of perceptions, behaviours and awareness related to obesity and obesity management among people living with obesity.5 days (Phase 1)120-minute OBB discussion with numeric and open-ended response (Phase 1)
Assessment of triggers for people with obesity to request medical therapy and expectations for both therapy available and their weight loss journey.5 days (Phase 1)120-minute OBB discussion with numeric and open-ended response (Phase 1)

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026