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Not yet recruitingNCT07605793Updated May 26, 2026

Reliability and Validity of Physical Performance Tests in Individuals With Obesity

An observational study in Obesity & Overweight, sponsored by Yunus Emre Tutuneken. Not yet recruiting. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-05-26.

Sponsored by Yunus Emre Tutuneken · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
55
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Obesity & Overweight

Keywords

  • Obesity
  • Performance test
  • Balance
  • Exercise capacity
03

In context

Obesity

6,297 studies on the registry are indexed under Obesity; 1,693 are open to participants now.

This study's planned enrollment of 55 is below the median of 135 across 1,283 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

This is the only study on the registry with Yunus Emre Tutuneken as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Individuals With Obesity

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

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)
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
55 participants (estimated)
Patient registry
No

Interventions

  • OtherPhysical 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 functional testing, participants will complete cardiopulmonary exercise testing (CPET) using the Modified Bruce Protocol to determine maximal oxygen consumption (VO₂max), computerized static and dynamic balance assessments using the PROKIN® system, and knee extensor muscle strength measurements using a hand-held dynamometer. No therapeutic intervention or treatment will be administered during the study.

06

What researchers measure

Primary outcomes

  1. 1-Minute Stair Climbing Test

    A performance-based functional test used to assess stair climbing ability and lower extremity functional capacity. The total number of completed stair cycles within 1 minute will be recorded.

    Time frame: 1 hour

  2. 40-Meter Fast-Paced Walk Test

    A walking performance test used to evaluate fast-paced gait speed and functional mobility. The time required to complete a total walking distance of 40 meters will be measured in seconds.

    Time frame: 1 hour

  3. 2-Minute Walk Test

    A functional endurance test used to assess ambulatory capacity. The total walking distance completed within 2 minutes will be recorded in meters.

    Time frame: 1 hour

  4. Timed Up and Go Test

    A functional mobility test used to assess dynamic balance and independent mobility. The time required to stand up from a chair, walk 3 meters, return, and sit down will be measured in seconds.

    Time frame: 1 hour

  5. 30-Second Sit-to-Stand Test

    A lower extremity functional strength and endurance test. The total number of sit-to-stand repetitions completed within 30 seconds will be recorded.

    Time frame: 1 hour

Secondary outcomes

  1. Cardiopulmonary Exercise Testing (VO₂max)

    A maximal exercise test performed using the Modified Bruce Protocol on a treadmill to assess aerobic exercise capacity. Maximal oxygen consumption (VO₂max) values will be recorded.

    Time frame: 1 hour

  2. Static Balance Assessment

    Balance performance will be evaluated using the PROKIN® computerized balance assessment system. Parameters related to postural stability and body sway during static tasks will be recorded

    Time frame: 1 hour

  3. Knee Extensor Muscle Strength

    Isometric knee extensor muscle strength will be measured using a hand-held dynamometer. Maximum voluntary contraction force will be recorded.

    Time frame: 1 hour

  4. Dynamic Balance Assessment

    Description: Balance performance will be evaluated using the PROKIN® computerized balance assessment system. Parameters related to postural stability and body sway during static and dynamic tasks will be recorded

    Time frame: 1 hour

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07605793
Lead sponsor
Yunus Emre Tutuneken
Responsible party
Yunus Emre Tutuneken (Istinye University, Istinye University) — Sponsor-investigator
First posted
May 26, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Oct 15, 2026 (estimated)
Completion
Oct 20, 2026 (estimated)
Last update
May 26, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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