The Immediate Effects of Post Isometric Relaxation Techniques

December 27, 2023 updated by: Sanem ŞENER, Bulent Ecevit University

The Immediate Effects of Post Isometric Relaxation Techniques In Hospital Employees With Neck Pain: A Randomised Control Trial

Aim: The aim of this study is to investigate the immediate effects of Post Isometric Relaxation (PIR) Technique on pain threshold, pain severity and joint range of motion of the cervical region in healthcare workers with neck pain.

Method: A total of 30 male and female participants aged 20-45 were randomly divided into two groups (Post Isometric Relaxation (PIR) Technique and Control Group). PIR group participants were under a single session of PIR application with 10 repetitions to m.supraspinatus, the upper part of the m.trapeze and m.levator scapula in addition to classical Swedish massage for neck and upper thoraric region. Control group participants received only classical Swedish massage to the cervical and upper thoracic region. Pain severity (Visual Analog Scale), Pain threshold (digital algometer), range of servical motion (goniometer) were measured at baseline and immediately after the single-session PIR Techniques.

Study Overview

Status

Completed

Conditions

Detailed Description

Neck pain is the second most common musculoskeletal problem in the world after low back pain in terms of disability and health expenditures. Occupational groups with the highest incidence of neck pain include those working in a hospital environment, office workers, and manual workers.

Post Isometric Relaxation Technique (PIR) is a Muscle Energy Technique (MET) and is used by physiotherapists to relax muscles, reduce pain and increase range of motion. The PIR Technique provides its neurological effects through autogenic inhibition, which results in relaxation in the agonist muscle by inhibiting contraction with the stimuli sent by the group Ib fibers originating from the Golgi tendon organ of the agonist muscle to the medulla spinalis during static stretching.

The aim of our study is to investigate the instantaneous effect of PIR Technique on pain threshold, pain intensity and joint range of motion (neck flexion, extension, right and left rotation, right and left lateral flexion) in hospital workers with neck pain.

This experimental study, which was planned as randomized and single-blind, was planned to be carried out with a total of 30 volunteer participants, male and female, working in a private hospital in Istanbul between 7 October 2022 and 10 December 2022.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kozlu
      • Zonguldak, Kozlu, Turkey, 67600
        • Zonguldak Bulent Ecevit University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 45 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • be a hospital worker
  • complaining of neck pain for at least 3 months
  • pain intensity at rest is 4 out of 10 according to VAS assessment
  • volunteer to participate in the study

Exclusion Criteria:

  • Having neck pain after trauma to the neck in the last 6 months
  • presence of neurological signs; neck pain that has spread to the arm and fingers
  • have had spinal surgery
  • shoulder pathology

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: PIR Group
PIR Group participants will be given a one-time PIR Technique for each of the neck and upper back muscles, right after the classical Swedish massage is applied to the cervical region and upper back area.
PIR is performed by first passively lengthening the muscle, then having the patient lightly contract (10-20% of maximum) against resistance for 5 seconds passively before exhaling and relaxing the muscle and repeated. The clinician then takes up the slack within the muscle and repeats the technique 3 to 5 times
classic Swedish massage for the cervical and upper thoracic region. Massage is a method that is applied to superficial soft tissues such as muscles, skin, ligaments and fascia and structures located under the superficial tissues and aims to relax.
Experimental: Control Group
Control group participants will receive classical Swedish massage only to the cervical and upper thoracic region.
classic Swedish massage for the cervical and upper thoracic region. Massage is a method that is applied to superficial soft tissues such as muscles, skin, ligaments and fascia and structures located under the superficial tissues and aims to relax.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain threshold assessment
Time Frame: 30 min
Digital algometer (JTECH Commander ™ Algometer with 0.5 cm2 tip) device was used. After training by showing the measuring instrument to the participants, pressure will be applied to a place outside the assessment area to introduce the feeling of pressure. He will be told to give a "stop" command as soon as the pain is first felt. This process will be applied 3 times to ensure that the participants adapt to the pressure to be applied during the evaluation. Before and immediately after the applications, all participants felt the pain for the first time with a speed of 10 N/s over the sensitive points of the m.trapezius pars descendes, m.levator Scapula, m.Rrhomboideus Major, M.Sternocleidomasteideus, suboccipital region, M. Infraspinatus, M. Multifidius muscles. will be increased so far. The measurement was terminated with the "Stop" command and a total of 3 measurements will be made and the average value seen on the screen will be recorded.
30 min
Pain severity assessment
Time Frame: 30 min
After explaining that '0 is no pain, 10 is the most severe pain', all participants will be asked to mark the intensity of pain they feel on the 10 cm horizontal Visual Analog Scale (VAS) before and immediately after the application.
30 min
Joint Range of Motion
Time Frame: 30 min
In order to evaluate the range of motion of the cervical vertebrae, measurements will be made before and immediately after the applications using a universal goniometer and according to Kendall-Mc Creary criteria. The fixed arm, pivot point and movable arm of the goniometer will be placed in certain reference areas in the measurement that starts when the participant is in a sitting position. Measurements of cervical flexion, extension, right and left lateral flexion, right and left rotation will be recorded after the participant's active movements, the angle value at the end of the movement, the active joint range of motion measurement.
30 min

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 7, 2022

Primary Completion (Actual)

November 7, 2022

Study Completion (Actual)

December 10, 2022

Study Registration Dates

First Submitted

October 12, 2022

First Submitted That Met QC Criteria

October 12, 2022

First Posted (Actual)

October 14, 2022

Study Record Updates

Last Update Posted (Actual)

December 28, 2023

Last Update Submitted That Met QC Criteria

December 27, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Immediate PIR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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