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Intermittent pneumatic compression for prolonged standing workers with leg edema and pain

Intermittent pneumatic compression for prolonged standing workers with leg edema and pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004163
Enrollment
20
Registered
2019-08-07
Start date
2018-09-12
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

Medical Device : The cross-design of three interventions proceeds as natural rest for 60 minutes group, Intermittent Pneumatic Compression application using sequential mode for 30 minutes + natural re

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women over 19 years of age 2) Participants with a long standing working career (* Long standing working group: Examples of work standing in "Health guide for standing and working workers" presented by the Korea Occupational Safety and Health Agency - Sales / cashiers of food and hospitality businesses such as large discount stores, food and hospitality workers, It is defined as casino dealers, workers in the laundry and hairdressing industry, assembly line workers, packing workers such as warehouses, construction workers, medical institutions, and education workers (schools, academies)) 3) Participants with leg pain and edema 4) Participants who stand for more than 8 hours 5) Participants who fully understand the purpose of the research and wish to participate in clinical research through voluntary consent

Exclusion criteria

Exclusion criteria: 1) Participants who do not match the age standards 2) A person who can not accurately express the pain area and the degree of cognitive decline 3) Participants who are suspected of having neurological diseases due to physical examination 4) Participants who appeal for sensory depression 5) Partcipaints who have had undergone surgery in the last 6 months 6) pregnant and lactating women, pregnant women with urine test, pregnant women during clinical trials 7) Any other person who is deemed inappropriate by the research supervisor

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale

Secondary

MeasureTime frame
Leg volume measurement;Measure leg circumference;Measure edema using body composition analyzer

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 4, 2026