Effectiveness of McKenzie and Trochanteric Belt With CT Therapy to Reduce Pain and Dysfunction of SI Joint

NCT ID: NCT05863390

Last Updated: 2023-05-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-01

Study Completion Date

2023-08-31

Brief Summary

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To determine the effectiveness of McKenzie exercises and trochanteric belt with conventional physical therapy to reduce pain and dysfunction of Sacroiliac joint (SIJ) in pregnant women

Detailed Description

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to findout the effectiveness of exercises in pregnant women

Conditions

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Sacroiliac Joint Dysfunction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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McKenzie exercise

Group Type EXPERIMENTAL

McKenzie exercise

Intervention Type BEHAVIORAL

routine simple McKenzie exercise

Trochanteric belt

Group Type OTHER

Trochanteric belt

Intervention Type DIAGNOSTIC_TEST

Trochanteric belt with conventional physical therapy

Interventions

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McKenzie exercise

routine simple McKenzie exercise

Intervention Type BEHAVIORAL

Trochanteric belt

Trochanteric belt with conventional physical therapy

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Pregnant patients with sacroiliac joint pain are included and participant patients with age group 18- to 35
* low back pain due to sacroiliac joint who suffer from sever pain during sitting and during positioning change when stand from sitting position are included

Exclusion Criteria

* Patients with age group of below 18 years and above 35 years
* Patients with disease of coagulopathy
* systemic infection
* skin infection over sacroiliac joint patients with history of allergies to injected medications.
* Patients with psoriasis
* inflammatory bowel disease
* peripheral arthritis
* Women with UTI complications are excluded.
* Women with respiratory issues are also excluded
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Superior University

OTHER

Sponsor Role lead

Responsible Party

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Muhammad Naveed Babur

DEAN

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abdul Wahab

Role: STUDY_CHAIR

Superior Uni

Locations

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• General Hospital. • Chaudhary Muhammad Akram Teaching and Research Hospital, University of Lahore Teaching Hospital, Shadman Medical Center, Services Hospital, Bahria International Hospital

Lahore, , Pakistan

Site Status RECRUITING

Countries

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Pakistan

Central Contacts

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Nargiza Saleem, DPT

Role: CONTACT

+923484080406

Other Identifiers

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DPT/Batch-Fall18/524

Identifier Type: -

Identifier Source: org_study_id

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