Effects Of Muscle Energy Technique Versus Mobilization

NCT ID: NCT04790500

Last Updated: 2021-09-23

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-14

Study Completion Date

2021-08-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim is to describe the severity of pain in postpartum female and management of sacroiliac joint pain and disability and define the effects of manual therapy on sacroiliac joint dysfunction and pain

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The aim is to describe the severity of pain in postpartum female and management of sacroiliac joint pain and disability and define the effects of manual therapy on sacroiliac joint dysfunction and pain in postpartum females and to check whether the amount of gaining range of movement is similar among postpartum female undergoing with mobilization therapy and with muscle energy technique.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sacroiliac Joint Dysfunction

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

mobilization technique

Group Type ACTIVE_COMPARATOR

mobilization technique

Intervention Type OTHER

Mobilization of sacroiliac joint which will increase the range of motion and reduction in pain and improvement in functional limitation.

Group B

muscle energy technique

Group Type EXPERIMENTAL

muscle energy technique

Intervention Type OTHER

Muscle energy technique it is known as active muscular relaxation technique. It helps in lengthening the shorten muscle and increasing range of restricted muscles

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

mobilization technique

Mobilization of sacroiliac joint which will increase the range of motion and reduction in pain and improvement in functional limitation.

Intervention Type OTHER

muscle energy technique

Muscle energy technique it is known as active muscular relaxation technique. It helps in lengthening the shorten muscle and increasing range of restricted muscles

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 20-40 year having unilateral back pain around or on sacral sulcus,
* Positive posterior pain provocation test for Sacroiliac joint dysfunction,
* Low back pain within six weeks of delivery
* Pain while sitting down, lying on the ipsilateral side of pain, or climbing stairs.
* Local tenderness of the posterior aspect of the sacroiliac joint
* Pain is usually localized over the buttock.
* Sharp, stabbing, and/or shooting pain which extends down the posterior thigh usually not past the knee.
* C-section

Exclusion Criteria

* Neurological deficit
* Spinal tumors
* Scoliosis,
* Underwent spinal surgery and prolapsed
* Intervertebral disc with or without radiculopathy
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Riphah International University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Anam Aftab, Phd*

Role: PRINCIPAL_INVESTIGATOR

Riphah college of rehabilitation and allied health sciences - Rawalpindi

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Pakistan railway hospital

Rawalpindi, Punjab Province, Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

REC/00846 Nusrat Javed

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.