Upper Extremity Pattern Exercises and Respiratory Functions

Sponsor
Ege University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06137534
Collaborator
(none)
20
1
1
2
10

Study Details

Study Description

Brief Summary

The study will be carried out with healthy students between the ages of 18-25 years who are studying at Ege University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation and who voluntarily agree to participate in the study. Informed consent form will be signed before the evaluation of the individuals. The study will be carried out as a single group with the inclusion of a total of 20 individuals. The students who volunteered to participate in the study will actively apply the selected PNF upper extremity patterns for 4 weeks and will be evaluated twice, before and after the application. Demographic information of the individuals; age, height, weight, gender, background, surname, smoking habit, alcohol habit, education level (class), sports habit, COVID-19 disease status and when it occurred will be recorded. Cosmed pulmonary function test device will be used to evaluate the respiratory function of the individuals, Oncomed brand electronic body weight and height measurement device will be used to calculate the body mass index. Body Image Perception Scale will be used for body image perception, Beck Depression Inventory will be used to evaluate psychological status, and Rosenberg Self-Esteem Scale will be used to evaluate sense of self.

Condition or Disease Intervention/Treatment Phase
  • Other: Proprioceptive Neuromuscular Facilitation Upper Extremity Pattern
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
It includes a single-group exercise application with volunteer healthy university students.It includes a single-group exercise application with volunteer healthy university students.
Masking:
None (Open Label)
Masking Description:
The researcher who performed the evaluation did not participate in the exercise sessions applied in the study. He/she does not have information about the application.
Primary Purpose:
Other
Official Title:
The Effect of Proprioceptive Neuromuscular Facilitation Upper Extremity Pattern Exercises on Respiratory Functions, Body Image, Self-Esteem and Psychological State
Anticipated Study Start Date :
Nov 10, 2023
Anticipated Primary Completion Date :
Nov 10, 2023
Anticipated Study Completion Date :
Jan 10, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Exercise Group

Proprioceptive neuromuscular facilitation upper extremity pattern exercises will be actively applied to 20 individuals in groups of 5 in a standing position for 30 minutes in each session 3 days a week for 4 weeks.

Other: Proprioceptive Neuromuscular Facilitation Upper Extremity Pattern
Proprioceptive neuromuscular facilitation upper extremity pattern exercises will be actively applied to 20 individuals in groups of 5 in a standing position for 30 minutes in each session 3 days a week for 4 weeks. PNF upper extremity patterns to be applied to the participants: Bilateral symmetrical flexion-adduction-external rotation. Bilateral symmetrical flexion-abduction-external rotation. Bilateral asymmetric right: flexion-abduction-external rotation, left: flexion-adduction-external rotation. Bilateral reciprocal (same diagonal) right: extension-adduction-internal rotation, left: flexion-abduction-external rotation. Bilateral reciprocal (same diagonal) right: flexion-adduction-external rotation, left: extension-abduction-internal rotation. Bilateral reciprocal (opposite diagonal) right: extension-adduction-internal rotation, left: flexion, adduction, external rotation.

Outcome Measures

Primary Outcome Measures

  1. Forced vital capacity (FVC) [At the beginning and at the end of 4 weeks of exercise.]

    It will be evaluated with Cosmed pulmonary function test device. The test will be performed according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria. The patient will be asked to take a deep breath in a sitting position and then exhale rapidly through the spirometer. Nasal clamp will be used during exhalation.

  2. Forced expiratory volume in the first second (FEV1) [At the beginning and at the end of 4 weeks of exercise.]

    It will be evaluated with Cosmed pulmonary function test device. The test will be performed according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria. The patient will be asked to take a deep breath in a sitting position and then exhale rapidly through the spirometer. Nasal clamp will be used during exhalation.

  3. Forced expiratory volume in the first second/Forced vital capacity (FEV1/FVC) [At the beginning and at the end of 4 weeks of exercise.]

    It will be evaluated with Cosmed pulmonary function test device. The test will be performed according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria. The patient will be asked to take a deep breath in a sitting position and then exhale rapidly through the spirometer. Nasal clamp will be used during exhalation.

  4. Forced expiratory flow between 25% and 75% of vital capacity (FEF25-75) [At the beginning and at the end of 4 weeks of exercise.]

    It will be evaluated with Cosmed pulmonary function test device. The test will be performed according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria. The patient will be asked to take a deep breath in a sitting position and then exhale rapidly through the spirometer. Nasal clamp will be used during exhalation.

  5. Body Image Perception Scale [At the beginning and at the end of 4 weeks of exercise.]

    The scale provides information about body image. The scale assesses satisfaction with 40 different body parts and functions. The scale has a minimum score of 40 and a maximum score of 200. A higher overall score on the scale indicates a higher negative judgement, while a lower overall score suggests a more positive evaluation.

Secondary Outcome Measures

  1. Rosenberg Self-Esteem Scale [At the beginning and at the end of 4 weeks of exercise.]

    The scale consists of 63 items. It is evaluated over 12 subscales and it is accepted that those who score 0-1 on the self-esteem subscale have high self-esteem, those who score 2-4 have medium self-esteem and those who score 5-6 have low self-esteem.

  2. Beck Depression Inventory [At the beginning and at the end of 4 weeks of exercise.]

    It is a scale developed to measure the behavioural findings of depression. As a result of the scoring, 0-9 points are interpreted as Minimal, 10-16 points as Mild, 17-29 points as Moderate, 30-63 points as Severe.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Not diagnosed with any chronic disease

  • No neurological problems

  • Has not had COVID-19 for at least 6 months

Exclusion Criteria:
  • Diagnosed with respiratory system diseases

  • Regular medication use

  • Suspected pregnancy

  • Individuals with rheumatic or neurological diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ege University Izmir Karsıyaka Turkey 35550

Sponsors and Collaborators

  • Ege University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ozden Gokcek, Principal Investigator, Ege University
ClinicalTrials.gov Identifier:
NCT06137534
Other Study ID Numbers:
  • 08/2023
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ozden Gokcek, Principal Investigator, Ege University

Study Results

No Results Posted as of Nov 18, 2023