- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06785805
Respiratory Functions, Aerobic Capacity and Quality of Life in Chronic Venous Insufficiency
Relationship Between Disease Severity, Pain, Lower Extremity Strength, Respiratory Functions, Aerobic Capacity and Quality of Life in Individuals With Chronic Venous Insufficiency
This study aims to retrospectively examine the dataset obtained from a previously conducted study titled 'Inspiratory muscle training in individuals with chronic venous insufficiency: randomized controlled trial'. The previously conducted study was a study investigating the effectiveness of the application, and the current study aims to clarify the gap in the literature with the relationship between the data obtained from the patients at the beginning of that study. This study will be conducted by re-examining the initial data of another study from which data was collected before and conducting new analyses.
H0: There is no relationship between disease severity, edema, pain, respiratory muscle strength, respiratory functions, aerobic capacity, lower extremity strength or quality of life in individuals with chronic venous insufficiency.
H1: There is a relationship between disease severity, edema, pain, respiratory muscle strength, respiratory functions, aerobic capacity, lower extremity strength or quality of life in individuals with chronic venous insufficiency.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Karabağlar/İzmir
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İzmir, Karabağlar/İzmir, Turkey, 35140
- Izmir Democracy University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being diagnosed with chronic venous insufficiency
- Agreeing to participate in the study
- Being 18 years of age or older
Exclusion Criteria:
- Presence of arterial diseases
- Presence of advanced cardiorespiratory diseases
- Presence of acute ulcers (< 3 months) and diabetic ulcers
- Being pregnant
- Presence of deep vein thrombosis
- Presence of active infection
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Individuals with Chronic venous insufficiency
Our prospective randomized controlled planned study named 'Inspiratory Muscle Training in Individuals with Chronic Venous Insufficiency: Randomized Controlled Study', which was approved by Izmir Democracy University Non-Interventional Clinical Research Ethics Committee on 21/06/2023 with the decision number 2023/08-02, was conducted.
Although 38 individuals diagnosed with CVI were included in the study, the study was completed with 30 individuals diagnosed with CVI who could complete the 6-week follow-up.
In the current study, which is a continuation of the previsious research; It is aimed to analyze the initial measurement results of 38 individuals diagnosed with CVI who were initially included in the study and to contribute these data to the literature with a retrospective cross-sectional study design.
Our new hypothesis is based on the examination of the correlation between these initial outcome measurements obtained from our previous study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Disease severity
Time Frame: From July 2023 to May 2024
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The disease severity (CEAP scores) of the individuals referred to the study were determined by the cardiovascular surgeon.
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From July 2023 to May 2024
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of Lower Extremity Strength
Time Frame: From July 2023 to May 2024
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The 30-second Sit-to-Stand Test was used on a chair to determine lower extremity strength and functional mobility.
Rikli et al. designed a 30-second sit-to-stand test in 1999 to evaluate individuals' dynamic balance and physical fitness lower extremity neuromuscular function levels.
During the test, the individual sat on a chair without back support, arms crossed over the body, which was the initial sitting position.
Then, the individual stood up and sat down repeatedly for 30 seconds.
The total number of correct standing ups during this period was recorded.
A higher number of repetitions indicates better physical performance.
Performing less than 10 repetitions of the movement in 30 seconds indicates lower extremity weakness.
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From July 2023 to May 2024
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Assessment of aerobic capacity
Time Frame: From July 2023 to May 2024
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The 6-minute walking test was performed according to ATS criteria and twice on the same day, half an hour apart.
Before the test, the subjects rested for at least 10 minutes, and before and after the test, oxygen saturation, heart rate, blood pressure, respiratory rate, dyspnea perception, fatigue and leg fatigue were recorded.
Oxygen saturation was assessed using a portable pulse oximeter, heart rate using a heart rate monitor, blood pressure using a sphygmomanometer, respiratory rate using a count of the breaths taken per minute, and fatigue, leg fatigue and dyspnea perception using the Modified Borg Scale.
The starting and ending points in the corridor where the test would be performed were determined and marked with cones.
The subjects were asked to walk as fast as they could at their own walking speed for 6 minutes on a 30-meter straight corridor.
In order to encourage the subjects, standard expressions were used for each minute during the test and the 6-MWT distance was recorded
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From July 2023 to May 2024
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Evaluation of respiratory functions
Time Frame: From July 2023 to May 2024
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A spirometer was used to evaluate respiratory functions.
Before the test, individuals rested for 15 minutes and during the rest, participants were told how to do the test, how to use a mouthpiece, when to inhale and exhale, and how to complete the test with maximum effort, and then they were shown a practical demonstration.
While individuals were sitting in a comfortable position in a chair with a back, a clip was placed on their noses and they were asked to bite the mouthpiece with their teeth and close their lips so that they would not allow air to escape.
During the test, individuals were asked to exhale until there was no air left in their lungs and they were allowed to follow the time on the monitor.
The tests were to be performed by the participants at least 3 times and it was ensured that the expiration time was at least 6 seconds and the plateau time was 1 second.
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From July 2023 to May 2024
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Respiratory muscle strength assessment
Time Frame: From July 2023 to May 2024
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Respiratory muscle strength was assessed with a spirometer.
The pressure was recorded during a few seconds of maximal inspiration (Müller maneuver) or expiration (Valsalva maneuver) through the mouth.
Maximum static inspiratory pressure was measured by having the patients take a rapid and deep inspiration at the residual volume after maximum expiration.
Maximum static expiratory pressure was measured by having the patients take a rapid and deep expiration at the total lung capacity after maximum inspiration.
The tests were performed in the sitting position using a nose clip.
The patients were verbally encouraged to achieve the best strength.
The measurement was repeated until a valid value was obtained in the patients.
If there was a difference of more than 5% or 5 cmH₂O between the consecutive measured values, the measurement was repeated.
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From July 2023 to May 2024
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Quality of life assessment
Time Frame: From July 2023 to May 2024
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The Chronic Venous Insufficiency Quality of Life Questionnaire (CIVIQ) was used to assess quality of life.
The questionnaire consists of 20 questions specific to Chronic Venous Insufficiency.
It consists of 4 parameters questioning physical, psychological, social status and pain.
Each question is scored according to a 5-item Likert scale.
Higher scores indicate better quality of life.
The Turkish validity and reliability study was conducted by Özdemir et al.
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From July 2023 to May 2024
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Pain Assessment
Time Frame: From July 2023 to May 2024
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Pain intensity was measured with the Numerical Rating Scale (SDS).
The maximum level of pain felt at rest and during activity was scored from 0 to 10.
A value of "0" indicates no pain, and a value of "10" indicates pain of the worst intensity.
The reliability and validity of the SDS was proven by Cleland et al., and the intraclass correlation coefficient (ICC) value was reported as 0.76.
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From July 2023 to May 2024
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Edema Assessment
Time Frame: From July 2023 to May 2024
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The edema in the lower extremity was assessed by measuring the circumference with a tape measure.
Each leg was recorded separately and the difference was calculated.
A flexible, non-elastic, 7 mm wide standard tape measure with a sensitivity level of 0.1 cm was used in circumference measurements.
The "0" (zero) end of the tape measure was wrapped around the area to be measured, with the other end in the left hand and the number on the "0" (zero) point noted.
During the measurement, care was taken to ensure that the "0" (zero) point of the tape measure and the measurement number were side by side, not on top of each other, and the measurement was performed with the patient in the supine position in order to ensure standardization in each measurement.
The circumference measurement values for each individual were converted to volumetric measurements by placing them in the Frustrum formula (truncated cone method).
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From July 2023 to May 2024
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Özlem Çinar Özdemir, Prof.Dr, Izmir Democracy University
Publications and helpful links
General Publications
- American Thoracic Society/European Respiratory Society. ATS/ERS Statement on respiratory muscle testing. Am J Respir Crit Care Med. 2002 Aug 15;166(4):518-624. doi: 10.1164/rccm.166.4.518. No abstract available.
- Kwon OY, Jung DY, Kim Y, Cho SH, Yi CH. Effects of ankle exercise combined with deep breathing on blood flow velocity in the femoral vein. Aust J Physiother. 2003;49(4):253-8. doi: 10.1016/s0004-9514(14)60141-0.
- Ozdemir OC, Tonga E, Tekindal A, Bakar Y. Cross-cultural adaptation, reliability and validity of the Turkish version of the Chronic Venous Disease Quality of Life Questionnaire (CIVIQ-20). Springerplus. 2016 Mar 31;5:381. doi: 10.1186/s40064-016-2039-2. eCollection 2016.
- Osada T, Katsumura T, Hamaoka T, Murase N, Naka M, Shimomitsu T. Quantitative effects of respiration on venous return during single knee extension-flexion. Int J Sports Med. 2002 Apr;23(3):183-90. doi: 10.1055/s-2002-23177.
- Tracz E, Zamojska E, Modrzejewski A, Zaborski D, Grzesiak W. Quality of life in patients with venous stasis ulcers and others with advanced venous insufficiency. Holist Nurs Pract. 2015 Mar-Apr;29(2):96-102. doi: 10.1097/HNP.0000000000000072.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IzmirDemocracy University
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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