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Search / Trial NCT04898491

Validity and Reliability Study of the Pain Indicator Behavior Scale-Brain Damage (ESCID-DC)

Launched by CANDELAS LOPEZ LOPEZ · May 18, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Pain Brain Injury Brain Damage Intensive Critical Unit Nursing

ClinConnect Summary

This clinical trial is studying a tool called the Pain Indicator Behavior Scale (ESCID), specifically adapted for patients with acquired brain injuries. The goal is to see if this scale can reliably measure pain in patients who cannot communicate verbally or through movement. By doing this, researchers hope to improve how we understand and treat pain in individuals with brain damage.

To participate in this study, individuals must be at least 18 years old and unable to communicate verbally or physically. They should also have an artificial airway (a tube that helps them breathe). Family members or representatives will need to give consent for participation. The trial is currently recruiting participants, and those who join can expect to help researchers gather important information that could lead to better pain management for patients with similar conditions in the future. It’s important to note that individuals with certain past medical conditions, such as severe brain injuries or dementia, won’t be eligible to participate.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age equal to or greater than 18 years.
  • 2. Inability to communicate verbally or motor.
  • 3. Have a artificial airway.
  • 4. Informed consent of the family member or representative of the patient.
  • Exclusion Criteria:
  • 1. Previous pathology of cognitive impairment.
  • 2. Previous brain injury.
  • 3. Previous psychiatric disorder.
  • 4. Previous dementia.
  • 5. Previous chronic substance abuse.
  • 6. Previous chronic diabetics.
  • 7. Previous spinal cord injury.
  • 8. Previous severe polyneuropathy (diagnosed or suspected).
  • 9. Confirmed diagnosis of brain death.
  • 10. Continuous infusion of muscle relaxants and / or barbiturate coma.
  • 11. Level of deep sedation (RASS -5).

About Candelas Lopez Lopez

Candelas Lopez Lopez is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative clinical studies. With a focus on ethical practices and regulatory compliance, the organization collaborates with healthcare professionals, researchers, and regulatory authorities to design and implement trials that address unmet medical needs. Candelas Lopez Lopez emphasizes rigorous scientific methodologies and patient-centered approaches, ensuring that all trials contribute valuable insights to the medical community while prioritizing participant safety and well-being.

Locations

Madrid, , Spain

Patients applied

0 patients applied

Trial Officials

Candelas López-López, PhD

Study Chair

Emergency and Trauma Intensive Care Unit. Hospital Universitario 12 de Octubre

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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