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NCT Number: NCT07344571

Investigating the Correlation Between Functional Constipation and Sacroiliac Joint Disorders

Constipation is a common gastrointestinal issue affecting individuals worldwide. Interferential therapy, a form of electrotherapy, has been suggested to have potential benefits in improving gastrointestinal motility and relieving constipation symptoms. Introducing of a new method like electronic cupping therapy with interferential therapy may optimize the therapeutic outcomes by potentially increasing bowel movements and improving overall gastrointestinal function.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

25 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Bassam Ahmed Nabil

October City, Giza Governorate, 6892, Egypt

About this study

Objective: The purpose of this study was to Investigate the correlation between functional constipation and sacroiliac joint disorders Methods: This study involved 200 patients with chronic constipation, consisting of 120 females and 80 males, ranging in age from 25 to 60 years. All participants were allocated into two groups: Group (A) patients with constipation, Group (B) patients without constipation

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inclusion Criteria:
  • history of Chronic Constipation (CC), as defined by either experiencing two or fewer Complete Spontaneous Bowel Movements (CSBMs) per week for a minimum of 6 consecutive months before the screening visit
  • Reporting a sensation of incomplete evacuation or straining during at least a quarter of their bowel movements (according to the generally accepted definition of constipation).
  • Patients must have had CC persisting for more than 6 months, failed to respond to or be intolerant of medical treatment for at least 3 months

Inclusion criteria

(for group B):

Not having functional constipation

Exclusion criteria

  • - pregnant or lactating women
  • Chronic Constipation (CC) resulting from anorectal malformations such as colorectal or anal organic lesions, pelvic floor disorders requiring surgical intervention as determined by the investigator (such as rectal prolapse, rectocele, or enterocele)
  • presence of implanted electronic devices like cardiac pacemakers, defibrillators, cardiac pumps, or spinal stimulators
  • CC attributable to medications or neurologic, endocrine, or metabolic conditions
  • prior history of partial colectomy; conditions like megacolon, megarectum, or colonic inertia
  • skin abnormalities that hinder the placement of electrodes
  • women lacking adequate contraception (hormonal or intrauterine device).

Treatment and study plan

Primary outcomes

  1. Distraction Test (SI Joint Gapping)

    Time frame: 6 months

    Position of patient: Supine. force: posterior-lateral force to both ASISs at same time results: pain in SI region

  2. Thigh Thrust Test

    Time frame: 6 months

    Position of patient: Supine, hip and knee of affected side flexed 90°. force: Stabilize opposite ASIS, apply posterior force through femur. result: Focal SI pain.

  3. Sacral Thrust Test

    Time frame: 6 months

    Position of patient: Prone. force: Apply an anterior shear force to sacrum (over S2). result: Reproduction of pain in SI region.

Sponsors and collaborators

Lead sponsor

Middle East University

Other

Registry information

Acronym: SIJ disorders

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jan 15, 2026
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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