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RecruitingNCT07870915Updated Oct 21, 2026

Relationship Between Interoception and Postural Control in Constipation-Predominant Irritable Bowel Syndrome

An observational study in Constipation and Irritable Bowel Disease, sponsored by Saglik Bilimleri Universitesi. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Saglik Bilimleri Universitesi · Observational

Updated Oct 21, 2026Now RecruitingSite recruiting status changed+1 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
128
Ages
18 Years to 45 Years
Sex
All
01

Study summary

This cross-sectional, observational, controlled comparative study aims to investigate the relationship between interoception and postural control in individuals with constipation-predominant irritable bowel syndrome (IBS-C) and to compare the findings with those of healthy individuals. Interoception will be assessed using the Multidimensional Assessment of Interoceptive Awareness-2 (MAIA-2), postural characteristics will be evaluated using the Corbin Posture Analysis, and stool type in the IBS-C group will be assessed using the Bristol Stool Scale.

Read the detailed description

This study is designed as a cross-sectional, observational, controlled comparative study. The study population will consist of individuals aged 18-45 years with a diagnosis of constipation-predominant irritable bowel syndrome (IBS-C) and healthy volunteers with similar age and sex characteristics.

The sample size was calculated using G*Power 3.1.9.7 based on a medium effect size (d=0.50), a significance level of 5% (α=0.05), and a statistical power of 80% (1-β=0.80). A total of 128 participants, with at least 64 participants in each group, are planned to be included.

After written informed consent is obtained, participants will complete a sociodemographic information form. Interoceptive awareness will be assessed using the Multidimensional Assessment of Interoceptive Awareness-2 (MAIA-2). Stool type will be evaluated using the Bristol Stool Scale in the IBS-C group, and posture will be assessed in all participants using the Corbin Posture Analysis.

The collected data will be analyzed using descriptive statistics, tests of normality, between-group comparison tests, correlation analyses, and multivariable regression analyses. Statistical significance will be set at p\<0.05.

02

Conditions studied

  • Constipation
  • Irritable Bowel Disease

Keywords

  • irritable bowel disease
  • posture
  • interoception
03

In context

Constipation

1,040 studies on the registry are indexed under Constipation; 139 are open to participants now.

This study's planned enrollment of 128 is above the median of 101 across 133 observational studies indexed under Constipation.

Browse Constipation studies →

Lead sponsor

Saglik Bilimleri Universitesi is the lead sponsor of 447 studies on the registry; 138 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals aged 18-45 years with a clinical diagnosis of constipation-predominant irritable bowel syndrome (IBS-C) and healthy volunteers with similar age and sex characteristics.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18-45 years.
  • For the IBS-C group, having a clinical diagnosis of constipation-predominant irritable bowel syndrome.
  • For the control group, having no history of gastrointestinal disease.
  • Voluntarily agreeing to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Having a neurological, rheumatological, or serious orthopedic disease.
  • Having a history of surgery that may affect posture.
  • Pregnancy.
  • Being unable to complete the assessments due to cognitive or communication impairment.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
128 participants (estimated)
Patient registry
No

Groups and cohorts

  • Constipation-Predominant Irritable Bowel Syndrome Group

    Individuals aged 18-45 years with a clinical diagnosis of constipation-predominant irritable bowel syndrome (IBS-C).

  • Healthy Control Group

    Healthy volunteers aged 18-45 years with similar age and sex characteristics to the IBS-C group and with no history of gastrointestinal disease.

06

What researchers measure

Primary outcomes

  1. Interoceptive Awareness

    Interoceptive awareness will be assessed using the Multidimensional Assessment of Interoceptive Awareness, Version 2 (MAIA-2), a 37-item self-report questionnaire with 8 subscales (Noticing, Not-Distracting, Not-Worrying, Attention Regulation, Emotional Awareness, Self-Regulation, Body Listening, Trusting). Each item is rated from 0 (never) to 5 (always), and the unit of measure is the mean score of each subscale (range 0 to 5). Higher scores indicate better interoceptive awareness.

    Time frame: Baseline (single assessment at study enrollment).

  2. Postural Characteristics

    Posture will be assessed by an examiner using the Corbin Posture Analysis, an observational posture evaluation in which body segments are rated against a standard postural alignment. The unit of measure is the total posture score (range: 0 to 20). Higher scores indicate worse posture.

    Time frame: Baseline (single assessment at study enrollment).

07

Study locations

1 of 1 sites recruiting
  • İstanbul Topkapı University
    Istanbul, Turkey (Türkiye)
    Recruiting
08

Updates

2 registry updates since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Oct 21, 2026
Sites
İstanbul Topkapı University is now Recruiting
Oct 21, 2026
Registered
First appeared on the registry
Oct 13, 2026
Show all 2 updates
  1. Oct 21, 2026
    Not yet recruiting→Recruiting
    İstanbul Topkapı University is now Recruiting
  2. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07870915
Responsible party
Gamze Altınkaynak (Assistant Professor, Istanbul Topkapi University) — Principal investigator
First posted
Oct 13, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Mar 31, 2027 (estimated)
Completion
Mar 31, 2027 (estimated)
Last update
Oct 21, 2026

Study contacts

Gamze Koyutürk, Asst Prof
Contact
gamzealtinkaynak@gmail.com
+905065798671
Mehmet Burak Uyaroğlu, Asst Prof
Contact
Gamze Koyutürk, Asst Prof
principal investigator · Topkapı University
Mehmet B Uyaroğlu, Asst Prof
study director · Fenerbahce University
Görkem Dizdar, Asst Prof
study chair · Topkapı University
Mehmet M Atasoy, Prof
study chair
Beyza Erdogmus, Dr
study chair

Oversight

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

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