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Identification of critical outcomes in sarcopenia: a Discrete Choice Experiment; Part: Questionnaire to assess patients’ preferences for outcomes in sarcopenia

Identification of critical outcomes in sarcopenia: a Discrete Choice Experiment; Part: Questionnaire to assess patients’ preferences for outcomes in sarcopenia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00015661
Enrollment
280
Registered
2018-10-09
Start date
2018-07-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

M62.50

Interventions

Group 1: sarcopenic patients are once questionned about the relative importance of 5 sarcopenia-related study outcomes for affected persons (mobility, quality of life, falls, activities of daily livin

Sponsors

Public Health, Epidemiology and Health Economics, CHU - Sart Tilman, Quartier Hôpital, University of Liège, Liège, Belgium
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 65 years or older with sarcopenia, i.e. low muscle mass ((assessed with bioelectrical impedance analysis): skeletal muscle mass index (SMMI) = SMM [in kg] / (height [in m])² = 10,75 kg/m² (men) / = 6,75 kg/m² (women)) in combination with low muscle strength (hand grip strength (dynamometry) < 30 kg (men) bzw. < 20 kg (women)) and/or slow walking speed (< 0,8 m/s)

Exclusion criteria

Exclusion criteria: not sarcopenic, refusal or unable to give informed consent, contraindication for bioelecrical impedance analysis, diagnosis of dementia or severe cognitive impairment or unable to understand task, severe depression, unable to sufficiently speak or understand German

Design outcomes

Primary

MeasureTime frame
the relative importance of 5 sarcopenia-related study outcomes for affected persons (mobility, quality of life, falls, activities of daily living, fatigue) by means of a discrete choice experiment (questionnaire with 13 scenarios)

Secondary

MeasureTime frame
differences in primary outcome between the 7 participating countries

Countries

Belgium, France, Germany, Italy, Spain, Switzerland, United Kingdom

Contacts

Public ContactSabine Goisser

Agaplesion Bethanien-Krankenhaus, Geriatrisches Zentrum der Universität Heidelberg

sabine.goisser@bethanien-heidelberg.de+4962213193348

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026