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5E Program for Preventing Venous Thromboembolism in Patients With Spinal Cord Disorders

K

Khon Kaen University

Status

Enrolling

Conditions

Venous Thromboembolism
Spinal Cord Injuries
Spinal Cord Diseases
Nurse's Role

Treatments

Behavioral: 5E program

Study type

Interventional

Funder types

Other

Identifiers

NCT06302478
KhonKaenU001

Details and patient eligibility

About

The goal of this quasi-experimental study is to examine the effects of a venous thromboembolism prevention program, or "5E" program, on the rates of venous thromboembolism in patients with spinal cord disorders. The main questions it aims to answer are:

  • Will participants receiving the 5E program have lower rates of venous thromboembolism compared to those receiving the usual care?
  • Will participants receiving the 5E program have lower scores of venous thromboembolism signs and symptoms compared to those receiving the usual care?
  • Will the average thigh and calf circumferences of participants before and after receiving the 5E program be different?

Participants in the intervention group will receive the 5E program, including

  • Education: health education regarding venous thromboembolism prevention
  • Elevation: leg elevation of 10-20 degrees
  • Exercise: ankle exercises
  • Enough fluid: adequate fluid uptake
  • Early application of intermittent pneumatic compression (IPC): IPC use within 48 hours after admission

Enrollment

42 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Caprini scores of 5-8 and >8
  • Able to communicate in the Thai language
  • Willing to participate in this study

Exclusion criteria

  • Alteration of consciousness
  • Experiencing complications, including neurogenic shock and autonomic dysreflexia
  • Being pregnant
  • Having fluid restriction

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

42 participants in 2 patient groups

5E Program
Experimental group
Description:
Participants in the 5E program group will receive 7-day nursing interventions.
Treatment:
Behavioral: 5E program
Usual Care
No Intervention group
Description:
Participants in the control group will receive 7-day usual care interventions, including health education regarding signs and symptoms of venous thromboembolism and IPC use if the participants experienced muscle power as grade 0.

Trial contacts and locations

1

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Central trial contact

Wiphawadee Potisopha, Ph.D.

Data sourced from clinicaltrials.gov

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