Global Overweight and oBesE (GLOBE) Patient Registry, Development and Implementation of Disease-specific: Severity, Quality of Life and Cost Instruments.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 500
- 试验地点
- 1
- 主要终点
- Development of a Disease-Specific Questionnaire
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •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.
排除标准
- •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.
结局指标
主要结局
Development of a Disease-Specific Questionnaire
时间窗: 2 months
次要结局
- Quality of Life Instrument(2 months)
研究者
Ravi Jandhyala
Dr
Medialis Ltd.