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Clinical Trials/NCT05936983
NCT05936983
Completed
Not Applicable

Comparison of Physical Fitness, Physical Activity Level, Depression and Quality of Life in Patients With Bipolar Disorder and Schizophrenia With Healthy Controls

Yeditepe University1 site in 1 country90 target enrollmentJune 2, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bipolar Disorder
Sponsor
Yeditepe University
Enrollment
90
Locations
1
Primary Endpoint
Waist measurement - Antropometric Measurements
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

According to the World Health Organization; Bipolar disorder ranks in the top 20 causes of disability among all medical conditions and 6th among mental disorders worldwide. Bipolar disorder is noted as a serious mental illness involving emotional ups and downs.

Detailed Description

Schizophrenia is a chronic mental disorder characterized by the appearance of both positive symptoms such as hallucinations and delusions and negative symptoms such as apathy and withdrawal, repetition of cognitive skills, and disorganization. In this study, it was aimed to compare physical fitness, physical activity level, depression and quality of life in bipolar disoder and schizophrenic patients with healthy individuals.

Registry
clinicaltrials.gov
Start Date
June 2, 2023
End Date
June 20, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Individuals diagnosed with bipolar disorder and schizophrenia by a physician according to DSM-5 criteria
  • Individuals with bipolar and schizophrenia between the ages of 30-55
  • Patients without any other accompanying psychiatric disorder
  • Patients who can communicate
  • Patients who agreed to participate in this study and gave informed consent

Exclusion Criteria

  • Patients with a psychiatric diagnosis other than bipolar and schizophrenia.
  • Pregnancy condition
  • Those who did not consent to participate in the study

Outcomes

Primary Outcomes

Waist measurement - Antropometric Measurements

Time Frame: 4 weeks

Waist measurement is measured from the narrowest area between the subcostal region and the iliac crest.

Abdomen measurement - Antropometric Measurements

Time Frame: 4 weeks

Abdomen measurement is measured at the level of the umbilicus without compression of the tissues.

Quick Inventory of Depressive Symptomatology (QIDS-SR16) scale

Time Frame: 4 weeks

QIDS-SR consists of 16 items each ranging from 0 to 3. It is scored by summing the highest response in each of a set of questions relating to sleep, weight and psychomotor symptoms and then adding the remaining items

The hip measurement - Antropometric Measurements

Time Frame: 4 weeks

The hip measurement is measured from the thickest part of the hip area.

Eurofit Test Battery

Time Frame: 4 weeks

A test-retest design was applied to test the reproducibility of several Eurofit test battery items. Supervision and measurement of the Eurofit test battery was performed by one trained mental health physical therapist following a standardized procedure. The Eurofit test battery included seven items and involved the assessment of the following measures: whole body balance, speed of limb movement, flexibility, explosive strength, static strength, abdominal muscular endurance and running speed.

International Physical Activity Questionnaire

Time Frame: 4 weeks

The IPAQ questionnaires list activities and request estimates of durations and frequencies for each activity engaged in over the past week. Durations are multiplied by known METs per activity and the results for all items are summed for the overall physical activity score. Scores for walking and for moderate and vigorous activities are sums of corresponding item scores. A sitting question is not included in physical activity score.

Study Sites (1)

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