The Effects of Cervical Stabilization Exercises on Pulmonary Functions and Respiratory Muscle Strength

January 8, 2018 updated by: birgül morkoç, Hacettepe University

The Effects of Cervical Stabilization Exercises on Pulmonary Functions and Respiratory Muscle Strength in Patients With Neck Pain

This study aims to assess the effects of stabilization exercises on pulmonary functions and respiratory muscle strength. 42 participants with neck pain enrolled the study.

Study Overview

Detailed Description

This study aims to assess the effects of stabilization exercises on pulmonary functions and respiratory muscle strength. 42 participants with neck pain enrolled the study. Participants were divided into two groups, stabilization group (n=21) and the control group (n=21). The participants underwent a total of 24 sessions of treatment thrice a week for eight weeks under the supervision of a physiotherapist.

Study Type

Interventional

Enrollment (Actual)

42

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

    • Altındağ
      • Ankara, Altındağ, Turkey, 06030
        • Institute of Health Sciences

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 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • neck pain longer than 3 months
  • patients between ages of 18 and 55

Exclusion Criteria:

  • patients with neurologic symptoms
  • patients with chronic pulmonary disease
  • previous surgery on cervical region

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
Other: the stabilization group
the stabilization group performed cervical stabilization exercises in lying, sitting, standing and on a swisball 3times a week during 8 weeks.
cervical stabilization exercises
Other: the control group
the control group performed conventional exercises including neck isometric, isotonic and posture exercises 3 times a week during 8 weeks.
conventional exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pulmonary functions
Time Frame: 8 weeks
pulmonary functions were measured with spirometric tests by two experienced physical therapists.
8 weeks
respiratory muscle strength
Time Frame: 8 weeks
respiratory muscle strength was measured using mouth pressure device by two experienced physical therapists.
8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Birgül Morkoç, PhD student, Hacettepe University

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)

December 1, 2015

Primary Completion (Actual)

April 30, 2017

Study Completion (Actual)

July 26, 2017

Study Registration Dates

First Submitted

November 22, 2017

First Submitted That Met QC Criteria

January 8, 2018

First Posted (Actual)

January 10, 2018

Study Record Updates

Last Update Posted (Actual)

January 10, 2018

Last Update Submitted That Met QC Criteria

January 8, 2018

Last Verified

January 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

none are planned to be shared

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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