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NCT Number: NCT07229027

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

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.

Recruiting

Interested in participating?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Online recruitment

Milton Keynes, MK12 5NW, United Kingdom

Location status: Recruiting

Location contact

Omolade Allen

CONTACT

[email protected]

+447502228066

About this study

Despite evidence on the burden of BMI >25, few disease-specific instruments comprehensively capture its multidimensional impact. Existing frameworks often target obesity (BMI ≥30) or patients on pharmacological or surgical therapy. Overweight and extremely obese populations are underrepresented, and economic and psychosocial dimensions are rarely integrated into severity staging.

This study, therefore, aims to systematically evaluate symptoms, comorbidities, HRQoL, and costs across the full spectrum of individuals with BMI >25, excluding those on GLP-1 therapy. Integrating clinician and patient perspectives will support the development of more inclusive severity measures and inform early intervention strategies.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.
  • Healthcare professional participant must meet the following criteria for inclusion in the study:
  • 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.

Exclusion criteria

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.

Treatment and study plan

Primary outcomes

  1. Development of a Disease-Specific Questionnaire

    Time frame: 2 months

Secondary outcomes

  1. Quality of Life Instrument

    Time frame: 2 months

Other outcomes

  1. Cost Implications of Obesity

    Time frame: 2 months

Study contacts

Contact information is provided by the study sponsor or research team.

Omolade Allen, PhD

CONTACT

[email protected]

+447502228066

Sponsors and collaborators

Lead sponsor

Medialis Ltd.

Industry

Registry information

Acronym: GLOBE

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 14, 2025
Registry last updated
Nov 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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