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Investigating the Correlation Between Functional Constipation and Sacroiliac Joint Disorders

Investigating the Correlation Between Functional Constipation and Sacroiliac Joint Disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07344571
Acronym
SIJ disorders
Enrollment
200
Registered
2026-01-15
Start date
2023-04-15
Completion date
2026-09-10
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Constipation

Keywords

constipation, sacroiliac joint disorders

Brief summary

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.

Detailed description

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

Interventions

None listed

Sponsors

Middle East University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
25 Years to 60 Years
Healthy volunteers
Yes

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).

Design outcomes

Primary

MeasureTime frameDescription
Distraction Test (SI Joint Gapping)6 monthsPosition of patient: Supine. force: posterior-lateral force to both ASISs at same time results: pain in SI region
Thigh Thrust Test6 monthsPosition of patient: Supine, hip and knee of affected side flexed 90°. force: Stabilize opposite ASIS, apply posterior force through femur. result: Focal SI pain.
Sacral Thrust Test6 monthsPosition of patient: Prone. force: Apply an anterior shear force to sacrum (over S2). result: Reproduction of pain in SI region.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026