Global Overweight and oBesE (GLOBE) Patient Registry, Development and Implementation of Disease-specific: Severity, Quality of Life and Cost Instruments.

NCT07229027 | Recruiting DMC

• 1 other identifier: MED 63
• Study Type: observational
• Target: 500
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Overweight (BMI > 25); Obesity & Overweight

Outcome Measures

Primary Outcomes (1)

• Development of a Disease-Specific Questionnaire

  2 months

Secondary Outcomes (1)

• Quality of Life Instrument

  2 months

Other Outcomes (1)

• Cost Implications of Obesity

  2 months

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients with BMI over 25 Healthcare professionals treating patients.

You may qualify if:

• 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.
• 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.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Medialis Ltd.: lead

Study Sites (1)

Online recruitment

Milton Keynes, MK12 5NW, United Kingdom

RECRUITING

MeSH Terms

Conditions

Overweight; Obesity

Condition Hierarchy (Ancestors)

Overnutrition; Nutrition Disorders; Nutritional and Metabolic Diseases; Body Weight; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Central Study Contacts

Omolade Allen, PhD

CONTACT

+447502228066; omolade@medialis.co.uk

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 60 Months
• Sponsor Type: INDUSTRY
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Dr

Study Record Dates

• First Submitted: November 13, 2025
• First Posted: November 14, 2025
• Study Start: November 1, 2025
• Primary Completion (Estimated): July 1, 2026
• Study Completion (Estimated): August 1, 2026
• Last Updated: November 14, 2025

Record last verified: 2025-11

Data Sharing

• IPD Sharing: Will not share

Locations

GB (1)