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Clinical Trials/NCT05982964
NCT05982964CompletedNot Applicable

Impact of Scapula Position on Functionality and Balance in People With Chronic Low Back Pain

Istanbul Medipol University Hospital1 site in 1 country81 target enrollmentStarted: July 31, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
81
Locations
1
Primary Endpoint
Examining the Scapular Position

Study Overview

Brief Summary

Chronic low back pain is defined as pain that lasts for more than 3 months or exceeds the expected recovery time.

Detailed Description

Chronic low back pain is defined as pain that lasts for more than 3 months or exceeds the expected recovery time.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Examining the Scapular Position

Time Frame: 1 day

The lateral scapular glide test was used to evaluate the scapula position. In the first position, the arms were relaxed at the sides, the shoulder was in the neutral position, in the second position the patient's hands were positioned around the waist and the humerus was brought to medial rotation and abduction of 45 degrees, and in the third position, the humerus was placed in maximal medial rotation and 90-degree abduction.

Pressure Pain Threshold Algometer

Time Frame: 1 day

The pressure algometer is a tool used to assess the pain threshold. The algometer used in this study is connected to a dial measuring the pressure in kilograms and pounds, and consists of a metal piston with a diameter of 1 centimeter at the tip, the smallest gap of which is 100 gr and 10 kg/cm².

Evaluation of Functionality

Time Frame: 1 day

The Oswestry Low Back Pain Disability Questionnaire (OBAEA) was used to examine functionality in patients with chronic low back pain. This survey consists of 10 questions in total. Each question has 6 options and ranges from 0 to 5. Participants are asked to mark the option that best fits their individual situation. While 50 is the highest score, it is evaluated as mild functional disability between 1 and 10 points, moderate functional disability between 11 and 30 points, and severe functional disability between 31 and 50 points.

Evaluation of Balance

Time Frame: 1 day

The static and dynamic postural stability of all individuals included in the study were evaluated with the Biodex Balance System (BDS). For dynamic stability measurement, a total of 3 tests were conducted, with the platform in dynamic position, with each period lasting 20 seconds, giving the participant a rest period of 10 seconds in between. Afterwards, the average of these 3 tests was obtained automatically by the device. In the results obtained, it is possible to interpret that as the score approaches 0, the balance is maintained, and as it moves away from 0, the balance is deteriorated.

Proprioception Evaluation

Time Frame: 1 day

An inclinometer is an instrument that records angular movements with respect to gravity. The inclinometer has many advantages such as precise measurement, digital display, and ease of use. In our study, inclinometer was used in the evaluation of proprioception. Measurements will be recorded in degrees.

Waist Awareness Assessment

Time Frame: 1 day

Fremantle Waist Awareness Questionnaire was used to evaluate low back awareness in the study. The Fremantle Waist Awareness Questionnaire is the only one that assesses body awareness about the waist. It consists of 9 questions in total and each question has a score ranging from 0-4. In total, the lowest 0 and the highest 36 points can be obtained. High scores indicate low back awareness.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Istanbul Medipol University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

hazal genc

Principal Investigator

Istanbul Medipol University Hospital

Study Sites (1)

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