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Not yet recruiting NCT07605793

Reliability and Validity of Physical Performance Tests in Individuals With Obesity

Observational Obesity & Overweight

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Physical Performance Tests.
Who it may be relevant to
Registry conditions: Obesity & Overweight. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Clinician-Friendly Physical Performance Tests in Individuals With Obesity: Reliability and Validity

Overview

This study aims to investigate the reliability and validity of practical performance-based physical function tests in individuals with obesity. Functional limitations such as reduced walking ability, impaired balance, and decreased lower extremity strength are common in people with obesity and may negatively affect daily activities and quality of life. Participants will complete several commonly used clinical functional tests, including the 1-Minute Stair Climbing Test, 40-Meter Fast-Paced Walk Test, 2-Minute Walk Test, Timed Up and Go Test, and 30-Second Sit-to-Stand Test. In addition, cardiopulmonary exercise testing, balance assessment, and knee extensor muscle strength measurements will be performed. The study will evaluate whether these simple and clinically applicable tests provide reliable results over repeated measurements and whether they are associated with objective indicators of physical function such as maximal oxygen consumption (VO₂max), balance performance, and muscle strength. The findings may help clinicians use practical and cost-effective tools to assess physical function in individuals with obesity.

Interventions

  • Other Physical Performance Tests
    Participants will undergo a series of standardized performance-based physical function assessments, including the 1-Minute Stair Climbing Test, 40-Meter Fast-Paced Walk Test, 2-Minute Walk Test, Timed Up and Go Test, and 30-Second Sit-to-Stand Test. Each test will be performed twice with standardized rest intervals between assessments. To evaluate test-retest reliability, the same functional tests will be repeated 5-7 days later under identical conditions and in the same order. In addition to f

Primary outcome measures

  • 1-Minute Stair Climbing Test [Time frame: 1 hour]
  • 40-Meter Fast-Paced Walk Test [Time frame: 1 hour]
  • 2-Minute Walk Test [Time frame: 1 hour]
  • Timed Up and Go Test [Time frame: 1 hour]
  • 30-Second Sit-to-Stand Test [Time frame: 1 hour]
Secondary outcome measures (4)
  • Cardiopulmonary Exercise Testing (VO₂max) [Time frame: 1 hour]
  • Static Balance Assessment [Time frame: 1 hour]
  • Knee Extensor Muscle Strength [Time frame: 1 hour]
  • Dynamic Balance Assessment [Time frame: 1 hour]

Eligibility criteria

Inclusion criteria

  • Body mass index (BMI) ≥ 30 kg/m²
  • Stable body weight during the last 3 months (less than ±2 kg change)
  • Ability to perform daily living activities independently

Exclusion criteria

  • History of cardiovascular disease
  • History of pulmonary disease
  • History of neurological disease
  • Musculoskeletal injury affecting lower extremity function
  • Presence of lower extremity prosthesis or severe deformity
  • Major surgery within the previous 6 months
  • Pregnancy
  • Postpartum period
  • Vestibular disorders affecting balance
  • Visual impairments affecting test performance
  • Hearing impairments affecting test performance
  • Cognitive impairment limiting understanding of instructions
  • Participation in strenuous physical activity before testing
  • Use of medications affecting cardiopulmonary responses (e.g., beta-blockers)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07605793 · 21

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗