Clinical Trials Directory

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UnknownNCT03338868

Serum Concentrations, Physical and Psychological Well-being in Metabolic Syndrome

Comparison of Serum Concentrations, Physical and Psychological Well-being in Patients Having Chronic Musculoskeletal Pain With and Without Metabolic Syndrome

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Ataturk Training and Research Hospital · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to investigate the serum concentrations, physical and psychological well-being characteristics in patients having chronic musculoskeletal pain with metabolic syndrome, and to compare patients without metabolic syndrome.

Detailed description

Metabolic syndrome (MetS) is a combination of metabolic risk factors such as impaired glucose level, dyslipidemia, hypertension, and central obesity. MetS has become a large public health issue with common interrelation to different accompanying disorders. Moreover, the link between MetS and musculoskeletal disorders has previously been demonstrated. Presence and prevalence of MetS in patients having musculoskeletal pain seems common and interrelated.However, to our knowledge, manifestations with clinical symptoms of MetS, some inflammatory markers via serum concentrations and physical and psychological health profiles of patients with seeking treatment from outpatient physical therapy for musculoskeletal pain conditions have not been researched up to now.

Conditions

Interventions

TypeNameDescription
OTHERBody compositionevaluated by Bodystat®1500 Bio-impedance Analyzer
OTHERPhysical activity levelassessed by the International Physical Activity Questionnaire-7
OTHERMusculoskeletal pain intensityevaluated with Visual Analog Scale
OTHERQuality of lifeassessed by the Nottingham Health Profile
OTHERPsychological Well-Beingassessed by the Hospital Anxiety and Depression Scale
DIAGNOSTIC_TESTBlood testsBlood tests included serum glucose, triglyceride, high-density lipoprotein cholesterol (HDL-C), and uric acid levels. Blood samples were collected from the patients after one night of fasting.

Timeline

Start date
2015-08-01
Primary completion
2017-11-30
Completion
2017-12-30
First posted
2017-11-09
Last updated
2017-11-17

Locations

2 sites across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT03338868. Inclusion in this directory is not an endorsement.