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Recruiting NCT06578091

Executive Function in Obese

Observational Obesity

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Obesity. 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
Turkey (Türkiye)
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

Effects of Executive Dysfunction on Physical Performance and General Well-Being in Obese Individuals

Overview

This study was planned to examine the effect of executive function problems on physical performance and general well-being in obese individuals.

Primary outcome measures

  • Executive function [Time frame: Baseline]
  • General Well-Being-Sleep Quality [Time frame: Baseline]
  • General Well-Being-Quality of Life [Time frame: Baseline]
  • Physical Performance-Timed Up and Go [Time frame: Baseline]
  • General Well-Being-Depression and Anxiety [Time frame: Baseline]
  • Physical Performance-Hand Grip Strength [Time frame: Baseline]
  • Physical Performance-Walking Speed [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

For the study group;

  • Individuals volunteering for the study with BMI ≥30 kg/m2
  • Individuals between the ages of 18-65 who volunteer to work
  • Individuals who scored 21 points and above in the cognitive assessment

For the control group;

  • Individuals volunteering for the study with BMI ≥30 kg/m2
  • Individuals between the ages of 18 and 65 who are willing to work
  • Scoring less than 21 points on the cognitive assessment

Exclusion criteria

  • Being at a mental level that cannot understand and answer the questions posed
  • Having a diagnosed neurological disease
  • Having had cancer within the last 2 years
  • Having major organ dysfunction
  • Having uncontrolled type 2 diabetes
  • Loss of vision, hearing

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
Cohort

Study locations

Turkey (Türkiye) · 1 center
  • Kutahya Health Sciences University — Kütahya

Identifiers

NCT: NCT06578091 · KSBU-2024/03-33

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗