- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05320484
Clinical Pilates Exercises On Posture In Patients With Shoulder-Neck Posture Problem
April 1, 2022 updated by: Meltem Uzun
The Effect Of Clinical Pilates Exercises On Posture In The Adult Patients With Shoulder-Neck Posture Problem: A Single-blind Randomized Controlled Trial
This study was designed to investigate the effect of clinic pilates exercise in adult patients whith shoulder- neck posture problem.
51 patients with forward head posture(FHP) and rounded shoulder posture(RSP) were included in this study and they were randomly divided into two groups as clinical pilates (group 1, n=26) and classical posture exercises (group 2, n=25).
Patients' demographics were recorded.
Deep neck fleksor muscle(DNFM) endurance was evaluated by pressure biofeedback unit (PBU).
Head, neck and shoulder posture were evaluated with wall- tragus, wall-acromion, tragus-acromion and chin-sternal notch distance.
Flexibility for shoulder region was evaluated with back scratch test.
The patients were evaluated both before the study and 6 weeks later.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Fifty-one individuals aged between 20-55 years whose FHP and RSP problems were determined by lateral posture analysis were included in the study.
However, a total of 12 individuals, 6 from each of the 2 groups, were excluded from the study because they could not complete the treatment sessions.
The study was completed with 39 participants.Individuals aged between 20-60 years, whose FHP and RSP problems were determined by lateral posture analysis, were included in the study.
Those with severe pain in the neck and shoulder girdle, scoliosis and neurological problems and those who had undergone any surgery in the relevant regions were not included in the study.
The individuals included in the study were randomized by lot and divided into 2 groups.
Group 1 was given clinical pilates exercises, and Group 2 was given a program consisting of classical posture exercises.
The exercise programs of both groups were performed by the same physiotherapist, and pre- and post-exercise evaluations were made by a different physiotherapist.
Study Type
Interventional
Enrollment (Actual)
39
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
-
-
Please Select
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Gaziantep, Please Select, Turkey, 27060
- SANKO 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 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- FHP and RSP problems were determined by lateral posture analysis
Exclusion Criteria:
- skoliosis
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: clinical pilates exercises
clinical pilates exercises applied to 1st group,for 3 days / week for 6 weeks.
|
clinical pilates exercises methods applied to the 1st group, classical posture exercises methods to the 2nd group for 3 days / week for 6 weeks.
|
Other: classical posture exercises
classical postural exercises applied to 2 nd group,for 3 days / week for 6 weeks.
|
clinical pilates exercises methods applied to the 1st group, classical posture exercises methods to the 2nd group for 3 days / week for 6 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Distance Measurements
Time Frame: 6 week
|
The right-left tragus-wall distance, right-left tragus-acromion distance, right-left wall-acromion distance, and chin-sternal notch distance were measured with the help of a tape measure.
|
6 week
|
The DNFM endurance
Time Frame: 6 week
|
The DNFM endurance of the cases was measured using a pressurized biofeedback unit (PBU
|
6 week
|
Shoulder Region Flexibility
Time Frame: 6 week
|
Back Scratch Test
|
6 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Meltem uzun, SANKO 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)
January 2, 2017
Primary Completion (Actual)
June 18, 2017
Study Completion (Actual)
July 18, 2017
Study Registration Dates
First Submitted
March 22, 2022
First Submitted That Met QC Criteria
April 1, 2022
First Posted (Actual)
April 11, 2022
Study Record Updates
Last Update Posted (Actual)
April 11, 2022
Last Update Submitted That Met QC Criteria
April 1, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- MeltemU
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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