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Recruiting NCT07488442

Efficacy of Cognitive Behavioral Therapy Administered in Patients With Dyssynergic Defecation

No phase Interventional Dyssynergic Defaecation

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
The protocol lists: Pelvic floor rehabilitation, Pelvic floor rehabilitation+cognitive behavioral therapy.
Who it may be relevant to
Registry conditions: Dyssynergic Defaecation. Basic parameters: 18 years — 55 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

An Evaluation of the Efficacy of Cognitive Behavioral Therapy Administered in Conjunction With Pelvic Floor Exercises in Patients With Dyssynergic Defecation

Overview

The aim of this study is to evaluate the effectiveness of cognitive-behavioral therapy when used in conjunction with lifestyle modifications and pelvic floor rehabilitation.

Interventions

  • Other Pelvic floor rehabilitation
    Relaxation and kegel exercises and biofeedback therapy
  • Behavioral Pelvic floor rehabilitation+cognitive behavioral therapy
    Relaxation and kegel exercises, biofeedback therapy and cognitive behavioral therapy

Primary outcome measures

  • Wexner Constipation Score [Time frame: first day of treatment and 5th week of treatment]
  • Constipation Severity Scale [Time frame: first day of treatment and 5th week of treatment]
Secondary outcome measures (2)
  • Bristol Stool Chart [Time frame: first day of treatment and 5th week of treatment]
  • Beck Depression Scale [Time frame: first day of treatment and 5th week of treatment]

Eligibility criteria

Inclusion criteria

  • A history of constipation lasting longer than one year
  • Chronic constipation as defined by the Rome IV criteria
  • Being between the ages of 18 and 55
  • Findings consistent with dyssynergic defecation on anorectal manometry and balloon defecography
  • Exclusion of organic and metabolic causes of chronic constipation

Exclusion criteria

  • Active bowel disease
  • Presence of an active anal fissure
  • History of major abdominal surgery
  • Presence of a neurological disorder
  • Presence of a serious psychiatric disorder
  • Use of medications that cause constipation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Ankara Etlik City Hospital — Ankara

Identifiers

NCT: NCT07488442 · AEŞH-EK-2025-314

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗