Patients Commitment to Compression Therapy (POMP)

February 9, 2023 updated by: Ihar Ihnatovich, Belarusian State Medical University
The study Patients Commitment to compression therapy (POMP) is observational, prospective. After the Phlebologist consultation after 1 month and 1 year, a telephone questionnaire is carried out for the patients included in the study with the involvement of a company specializing in conducting a telephone questionnaire. Patients will be interviewed about the implementation of the doctor's recommendations regarding compression therapy over a period 1 month and 1 year.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Phlebologists will include in the study patients who have consulted and need compression therapy using a compression hosiery. Patients are recommended compression hosiery that meet RAL-GZ 387, Oeko-Tex Standart 100. At the same time, the design of this study does not provide for restrictions on the acquisition by patients of other type compression hosiery.

Inclusion of patients in the study is carried out only after obtaining written informed consent from them for data registration and subsequent telephone questionnaires. Demographic, anamnestic, sociological data, such as educational level, labor characteristics (heavy physical labor, prolonged orthostasis, prolonged sitting position) recorde in the patient's individual card. Women provide information on the number of births, menopause, use of hormone replacement therapy at the time of the study. A diagnosis performed for each lower limb according to only the clinical part of the CEAP classification without other details. The phlebologist individually for each patient determines the mode of wearing compression hosiery. In addition to compression therapy, it is possible to prescribe any other type of drug and / or surgical treatment. In the subsequent analysis, data on the lower limb with more severe manifestations of venous insufficiency are used.

Table 1. Main characteristics of the patients included in the study Class С Age, years Sex Мail/Femail University education Yes / No Prolonged orthostasis Yes / No Hard physical labor Yes / No Prolonged sitting position Yes / No Family history of Chronic Vein Disease Yes / No A history of Venous Thromboembolism Yes / No Smoking Yes / No History of childbirth (among women) Number 0-…. Hormonal contraception / hormone replacement therapy (among women) Yes / No

1 month and 1 year after the consultation patients will interrogate about the implementation of the doctor's recommendations regarding compression therapy (Tabl. 2) Table 2. Questions included in the telephone survey You have been prescribed compression hosiery. Have you bought it?

  • Did not buy
  • Bought immediately after a visit to the doctor
  • Not immediately bought (after how many days) Which product did you buy?
  • Knee socks
  • Stockings
  • One-leg stocking with zipper at the waist (monostocking)
  • Tights Do you follow the recommended doctor's regimen for wearing compression hosiery? - ---
  • Yes
  • No

If you did not comply with the compression hosiery pattern, then why?

  • Too difficult to put on / take off
  • Uncomfortable to wear
  • Hot to wear
  • Itching when used
  • Ugly
  • Does not help
  • It gets worse when I start wearing
  • I can not wash the product every day
  • Other (with explanation) Did you wear compression hosiery before being included in the study?
  • Yes
  • No What kind of compression hosiery had you wear before you entered the study?
  • Knee socks
  • Stockings
  • One-leg stocking with zipper at the waist (monostocking)
  • Tights Compression class
  • 1
  • 2
  • 3

How are you satisfied with the effect of the using compression hosiery? Score in points from 0 to 10, where 10 is the maximum level of satisfaction

How are you satisfied with the comfort of the using compression hosiery? Score in points from 0 to 10, where 10 is the maximum level of satisfaction

How are you satisfied with the quality of the using compression hosiery? Score in points from 0 to 10, where 10 is the maximum level of satisfaction

Study Type

Observational

Enrollment (Actual)

400

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

      • Minsk, Belarus, 220116
        • Belarusian State Medical University
    • Dzerzhinski Ave., 83
      • Minsk, Dzerzhinski Ave., 83, Belarus, 220116
        • Educational Institution"Belarusian State Medical 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

18 years to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

patients with varicose veins of the legs

Description

Inclusion Criteria:

  • varicose veins of the legs and compression therapy prescribed by a phlebologist

Exclusion Criteria:

  • hearing impairment, which could interfere with a telephone questionnaires

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients who have consulted and need compression therapy using
1) age from 18 to 75 years; 2) compression therapy prescribed by a phlebologist. The exclusion criterion is hearing impairment, which could interfere with a telephone questionnaires.
patients will be prescribed compression therapy for varicose veins of the legs using compression stockings

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
number of patients who will follow prescribed compression therapy and recommended doctor's regimen for wearing compression hosiery
Time Frame: 1 month
1-followed 2- did not followed
1 month
number of patients who will follow prescribed compression therapy and recommended doctor's regimen for wearing compression hosiery
Time Frame: 1 year
1-followed 2- did not followed
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
number of patients who will satisfy with the effect,comfort and quality of the using compression hosiery
Time Frame: 1 month
Score in points from 0 to 10, where 10 is the maximum level of satisfaction
1 month
number of patients who will satisfy with the effect,comfort and quality of the using compression hosiery
Time Frame: 1 year
Score in points from 0 to 10, where 10 is the maximum level of satisfaction
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ihar Ihnatovich, Prof, Belarusian State Medical University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

October 1, 2019

Primary Completion (ACTUAL)

January 1, 2020

Study Completion (ACTUAL)

January 26, 2021

Study Registration Dates

First Submitted

September 16, 2019

First Submitted That Met QC Criteria

September 18, 2019

First Posted (ACTUAL)

September 20, 2019

Study Record Updates

Last Update Posted (ACTUAL)

February 10, 2023

Last Update Submitted That Met QC Criteria

February 9, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 1-30082019

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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