- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03395054
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
Status
Completed
Conditions
Intervention / Treatment
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO 151623-09
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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