Therapeutic Exercises and Stabilization Exercises Given After Manual Therapy

March 19, 2021 updated by: Emine Atıcı, Okan University

Comparison of the Effects of Therapeutic Exercises and Stabilization Exercises After Manual Therapy in Patients With Non-Specific Chronic Neck Pain

The study was conducted to determine and compare the effects of the therapeutic exercises and stabilization exercises given to the patient after the manual therapy session on pain, neck range of motion, daily living activities and quality of life.

Study Overview

Status

Completed

Intervention / Treatment

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

      • İstanbul, Turkey, 34959
        • Emine

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

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Between the ages of 18-65,
  • having neck pain for 3 months or longer,
  • was diagnosed with chronic neck pain by a specialist.

Exclusion Criteria:

  • People with neurological diseases,
  • who had previous surgery in the cervical region,
  • who had medulla spinalis tumors,
  • vascular pathologies,
  • fractures,
  • osteoporosis,
  • rheumatoid arthritis problems were not included in the study.

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
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Stabilization Exercise Group
After manuel therapy, the patients were allocated into two groups as Stabilization Exercise Group and Therapeutic Exercise Group randomly.
EXPERIMENTAL: Therapeutic Exercise Group
After manuel therapy, the patients were allocated into two groups as Stabilization Exercise Group and Therapeutic Exercise Group randomly.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analogue Scale
Time Frame: 1 minute
The Visual Analog Scale (VAS) was developed to transform values which cannot be measured numerically to a numerical form. The patient is instructed to mark the severity of pain on a line marked at one end as 0=no pain to 10=intolerable pain, thereby providing the level of pain in a numerical form
1 minute
Range of motion
Time Frame: 10 minute
Devices to measure range of motion in the joints of the body include the Goniometer and Inclinometer which use a stationary arm, protractor, fulcrum, and movement arm to measure angle from axis of the joint. We measured neck flexio, extantion and rotation
10 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lateral Scapular Shift Test
Time Frame: 5 minute
This test involves measuring the distance from the inferior angle of the scapula to the nearest vertebral spinous process using a tape measure or goniometer in three positions: shoulder in neutral, shoulder at 40-45 degrees of coronal plane abduction with hands resting on hips, and the shoulder at 90 degrees abduction with the arms in full internal rotation
5 minute
Neck Disability Index
Time Frame: 3 minutes
The Neck Disability Index (NDI) is a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain
3 minutes
Bournemouth Neck Pain Questionnaire
Time Frame: 5 minutes
Neck Bournemouth Questionnaire (NBQ) was created by Bolton and Humphreys due to the necessity of an evaluation measure to various health domains, such as pain, function, incapacity and psychological and social aspects of patients with neck pathologies. This tool is easily applied, reproducible and responsive to clinical alterations, which makes it adequate to be used for scientific research and clinical practice to monitor the pathology progression and to assist treatment planning.
5 minutes

Collaborators and Investigators

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

Sponsor

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)

February 1, 2020

Primary Completion (ACTUAL)

September 30, 2020

Study Completion (ACTUAL)

December 1, 2020

Study Registration Dates

First Submitted

March 18, 2021

First Submitted That Met QC Criteria

March 18, 2021

First Posted (ACTUAL)

March 22, 2021

Study Record Updates

Last Update Posted (ACTUAL)

March 23, 2021

Last Update Submitted That Met QC Criteria

March 19, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 005

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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