MedPath

Awareness, Care & Treatment In Obesity Management

Completed
Conditions
Obesity
Interventions
Other: No treatment given
Registration Number
NCT05690789
Lead Sponsor
Novo Nordisk A/S
Brief Summary

ACTION France is a cross-sectional, observational, descriptive, and exploratory survey-based study without collection of laboratory data. The study is not related to any specific treatment options or pharmaceutical product. Collection of data will be performed via quantitative online survey by a third-party vendor.

The goal of this study is to provide insights to drive awareness around the needs of People Living with Obesity (PLwO) and Health Care Professionals (HCPs) involved in obesity treatment and management.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1688
Inclusion Criteria

People Living with Obesity

  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, aged above or equal to 18 years at the time of signing informed consent Lives in France
  3. Current BMI based on self-reported height and weight of at least 30 kg/m^2

Health Care Professionals

  1. Informed consent before any study related activities (study-related activities are any procedure related to recording/collection of data according to protocol)
  2. Male or female, aged greater than or equal to 18 years at the time of signing informed consent.
  3. Physician with a license to practice
  4. Specialty is not surgeon (including bariatric or plastic surgeon)
  5. Practices in France
  6. In clinical practice greater than or equal to 2 years
  7. Spends at least 70 percent time in direct patient care
  8. Has seen at least 100 patients in past month
  9. Has seen at least 10 patients in past month needing weight management defined as: a patient with a BMI greater than or equal to 30 kg/m^2 with or without comorbidities.

Employers

  1. Informed consent before any study related activities (study-related activities are any procedure related to recording/collection of data according to protocol)
  2. Age 18 years old or older
  3. works in France
  4. Company offers health insurance benefits
  5. Responsible for making or influencing decisions about employee benefits plan or health and wellness programs
  6. works in a company that has at least 20 employees
  7. not affiliated with pharma, MR or advertising firms
Exclusion Criteria

People Living with obesity

  1. Previous participation in this study. Participation is defined as having given online consent in this study
  2. Currently pregnant
  3. Participates in intense fitness or body building programs
  4. Has had significant, unintentional weight loss (due to major injury, illness, etc) in the past 6 months
  5. Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation

Health Care Providers

  1. Previous participation in this study. Participation is defined as having given informed consent in this study.
  2. Unwillingness, inability, or language barriers precluding adequate understanding or cooperation.

Employers

  1. Previous participation in this study. Participation is defined as having given informed consent in this study.
  2. Unwillingness, inability, or language barriers precluding adequate understanding or cooperation.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
People / Person Living with Obesity (PLwO)No treatment givenFrom online, general population consumer panels
Health Care Professionals (HCPs)No treatment givenHCPs treating people who have obesity
EmployersNo treatment givenSingle-selection response from defined list
Primary Outcome Measures
NameTimeMethod
Attitudes toward prescription weight loss medication and surgeryDay 1-day of survey

5-point Likert scale

1=strongly disagree to 5=strongly agree

Weight loss motivatorsDay 1-day of survey

Multi-select from defined list

Obesity attitudesDay 1-day of survey

5-point Likert scale

1=strongly disagree to 5=strongly agree

Proportion of PLwO / participants who made serious weight loss effortDay 1-day of survey

Percentage of participants

Effective weight loss methodsDay 1-day of survey

Multi-select from defined list

Obesity and weight managementDay 1-day of survey

5-point Likert scale

1=strongly disagree to 5=strongly agree

Weight loss barriersDay 1-day of survey

Multi-select from defined list

Response to weight loss discussionsDay 1-day of survey

Single select from defined list

Degree to which healthcare and society is meeting needs of people living with obesityDay 1-day of survey

5-point Likert scale

1=strongly disagree to 5=strongly agree

Secondary Outcome Measures
NameTimeMethod
Top factors for improving weight loss outcomesDay 1-day of survey

Multi-select from defined list

Ways participants receive information on weight loss managementDay 1-day of survey

Multi-select from defined list

Most helpful information for participants for weight lossDay 1-day of survey

Multi-select from defined list

Responsibility for improving health of people living with obesityDay 1-day of survey

Multi-select from defined list

Most helpful support for weight lossDay 1-day of survey

Multi-select from defined list

Types of weight management goalsDay 1-day of survey

Multi-select from defined list

Effectiveness of guidelines for treating obesityDay 1-day of survey

5-point Likert scale

1=strongly disagree to 5=strongly agree

Trial Locations

Locations (1)

Novo Nordisk Investigational Site

🇫🇷

Puteaux, France

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