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Clinical Trials/NCT04822428
NCT04822428CompletedNot Applicable

Effect of Visceral Osteopathic Manipulations on Low Back Pain Caused by Visceral Dysfunctions

Cairo University1 site in 1 country40 target enrollmentStarted: August 20, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Modified Schober's test (MST)

Study Overview

Brief Summary

Forty female patients with age ranging from 30-40 years old were suffering from low back pain due to visceral dysfunctions participated in this study. They were recruited from a private clinic. They were assigned into two groups equal in number; Group (A): included twenty patients who received osteopathic manipulative techniques, 1 session per week for 3 weeks, and Group (B): included twenty patients who received only analgesic drugs.

Detailed Description

Twenty patients received osteopathic manipulative techniques including Suboccipital release technique, diaphragmatic release.,mesentery release and Colonic manipulation were applied to the study group according to the patients' needs.

The treatment program comprised a total of 3 sessions for 3 weeks at one session per week for an average of 50 minutes per session. Twenty patients in the second group (control ) took only analgesics during the three weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
30 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Non-specific low back pain for more than 12 weeks

Exclusion Criteria

  • •Malignant tumor
  • •Pregnancy
  • •Acute ischemic bowel disease,
  • •Intestinal obstruction,
  • •surgery in the last six months

Arms & Interventions

study group(A)

Experimental

Group (A): included Twenty patients who received osteopathic manipulative techniques, 1 session per week for 3 weeks.

Intervention: Osteopathic manipulation (Other)

Control group(B)

No Intervention

Group (B): included twenty patients who received analgesic drugs only.

Outcomes

Primary Outcomes

Modified Schober's test (MST)

Time Frame: change from baseline to after 3 weeks

the participant stood erect while the lumbosacral junction was marked as indicated by the dimples of Venus. For measuring the MST, we put a mark 5 cm below and 10 cm above the junction. The participant was asked to bend forward as far as possible and the stretched distance of these two points was measured as the MST value.

The Oswestry Disability Index (ODI)

Time Frame: change from baseline to after 3 weeks

(ODI) consists of 10 items on the degree of severity to which back (or leg) trouble has affected the ability to manage in everyday life.

The visual analog scale (VAS)

Time Frame: change from baseline to after 3 weeks

The patient determined the pain intensity on a 10 cm scale marked with points ranging from predetermined no pain and excruciating pain

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Heba Ahmed Ali Abdeen

Assistant professor

Cairo University

Study Sites (1)

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