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Clinical Trials/NCT06621160
NCT06621160
Completed
Not Applicable

Investigation of Spinal Posture and Anthropometric Characteristics of Women with Chronic Constipation

Ondokuz Mayıs University1 site in 1 country80 target enrollmentMarch 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Constipation
Sponsor
Ondokuz Mayıs University
Enrollment
80
Locations
1
Primary Endpoint
Anthropometric Characteristics
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of this study was to compare the spinal posture and anthropometric characteristics of women with Chronic Constipation (CC) and healthy women.

Registry
clinicaltrials.gov
Start Date
March 1, 2022
End Date
October 1, 2023
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Ondokuz Mayıs University
Responsible Party
Principal Investigator
Principal Investigator

Deniz Çakır

Principal Investigator

Ondokuz Mayıs University

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria for women with chronic constipation:
  • Constipation according to Rome IV criteria between the ages of 18-65
  • Volunteer
  • Inclusion criteria for healthy women:
  • No constipation according to Rome IV criteria between the ages of 18-65
  • Volunteer

Exclusion Criteria

  • Cancer, neurological disease, serious or uncontrolled systemic or metabolic disease
  • Being pregnant
  • Having a mental problem that will prevent cooperation
  • Having alarm symptoms over the age of 50
  • Having a diagnosis of secondary constipation
  • Being BMI\>35
  • Having megacolon/megarectum and inactive (lazy) bowel syndrome
  • Having had colostomy surgery
  • Having a history of recent abdominal surgery
  • Having an open wound or local tumor in the abdominal region

Outcomes

Primary Outcomes

Anthropometric Characteristics

Time Frame: 1 year

The individuals anthropometric characteristics were assessed with triceps, subscapula, suprailiac and calf skinfold thickness, humerus and femur epicondyle diameter, biceps and calf circumference measurements. Triceps skinfold thickness, subscapula skinfold thickness, suprailiac skinfold thickness, calf skinfold thickness were measured with skinfold caliper; humeral epicondyle diameter, femoral epicondyle diameter were measured with mechanical caliper, biceps circumference, calf circumference were measured with tape measure. Skinfold thickness measurements were performed by the same person. The measurements were taken from the dominant side of the individuals. The measurements were performed on healthy skin and the areas to be measured were marked with a marker. The individuals were asked to relax their muscles while the measurement was performed. The skin in the marked areas was pulled up by pinching between the index finger and thumb, and the skinfold caliper was placed 1 cm below t

Spinal Posture

Time Frame: 1 year

The individuals spinal postures were assessed with the Spinal Mouse. Individuals were informed about the device used and the duration of the assessment. Before the measurement, the positions in which the assessment would be made and how to do these positions were explained to the individuals. Then, a trial measurement was made once. The individuals\' demographic information was entered into the computer software. Individuals were asked to stand symmetrically with their vertebral columns exposed, to take off their shoes and step onto the mat, and to distribute their weight equally on both feet on a flat surface. Spinal processes starting from C7 to S3 were determined by the physiotherapist and marked with a felt-tip pen. For measurements, the Spinal Mouse device was moved from C7 to the S3 spinous process.

Study Sites (1)

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