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Comparison of intermittent pneumatic compression device and compression stockings for workers with leg edema and pain after prolonged standing: a prospective crossover clinical trial

Comparison of intermittent pneumatic compression device and compression stockings for workers with leg edema and pain after prolonged standing: a prospective crossover clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005383
Enrollment
40
Registered
2020-09-08
Start date
2019-12-19
Completion date
Unknown
Last updated
2021-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : Natural rest treatment group: natural rest during intervention after causing edema from wor Compression stocking treatment group: a natural rest treatment after daily work during intervention

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women over 19 years old 2) Participants who have a job performing work in a standing position for a long time(* Occupational group working for a long period of time: An example of the work of standing in the “Health Guide for Standing Workers” proposed by the Korea Health and Safety Agency – Salespersons/cashiers in wholesale and retail businesses such as large discount marts, food and lodging business workers, highway rest area salespeople, casino dealers, laundry and hairdressing business workers, assembly line workers, logistics warehouse workers, packaging workers, construction workers, medical institutions, educational work ( School, academy), etc.) 3) Those with leg pain and edema 4) Those who stand for more than 8 hours 5) Those who fully understand the research purpose and procedure and wish to participate in clinical research through voluntary consent

Exclusion criteria

Exclusion criteria: 1) Those who do not match the age criteria 2) Those who cannot accurately express the pain area and degree due to cognitive decline 3) Participants with ankle brachial index test result of 0.8 or less and suspected peripheral arterial obstruction 4) Those diagnosed with deep vein thrombosis by Doppler ultrasound of the lower extremities 5) Those with an underlying medical history, such as kidney disease or heart disease 6) Those who complain of decreased senses 7) Those who have had lower limb surgery within the last 6 months 8) Persons who are deemed unsuitable for participation by other research directors

Design outcomes

Primary

MeasureTime frame
Visual analogue scale

Secondary

MeasureTime frame
lower limbs circumference;The circumference of the lower limbs(the back of the foot, 2cm above the ankle, 10cm below the knee, 10cm above the knee, 20cm above the knee).;edema level measurement

Countries

Korea, Republic of

Contacts

Public ContactSeung-Rok Kang

Jeonbuk National University Hospital

srkang@mdctc.or.kr+82-63-259-3458

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 11, 2026