Bedside Evaluation of Edema

NCT ID: NCT03296085

Last Updated: 2023-06-28

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 1 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-11-30
• Study Completion Date: 2022-12-30

Brief Summary

Edema, commonly called swelling, is a common medical condition, with many causes. Clinicians generally find edema by pressing against a patient's skin, usually on the feet or shins, and observing how much dimpling there is in the skin. Most clinicians estimate the amount on a scale of mild to severe, or perhaps state the amount as 1 to 4. There is little agreement between observers, and it is hard to judge different clinicians' use of these scales. The first part of this experiment will demonstrate this inconsistency. After clinicians are shown a new technique for measuring edema, the second part of the study will show more accurate and consistent measurements. This will help clinicians to measure edema better, and to communicate their findings to other clinicians more effectively.

Detailed Description

The research team will recruit as many clinicians who are conveniently available for the study. Clinicians will include attending physicians from any specialty, residents, medical students, physician assistants, physician assistant students, nurses, certified nurse practitioners, and certified nurse practitioner students.

Once patients and clinicians have been recruited, the research team will maintain a list of the patients and a grid of which clinicians are to examine which patients. Each clinician will be given a data collection sheet, listing the patients' room numbers, and a grid for recording results for each of the patient's affected limb(s). The first data collection sheet (before instruction on the quantitative method) will just show a blank free text field so that clinicians can record their results as they normally do.

After instruction in the novel quantitative technique, the clinicians will receive another data collection sheet now indicating the intent to have the clinicians record their findings in millimeters.

The expectation is that a minimum of 6 examiners will determine the extent of edema on at least 38 limbs. If possible, the research will continue until approximately 100 limbs have been examined by a total of at least 10 to 20 clinicians.

Conditions

Edema

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

Exam for quantity of edema

There is no intervention

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Currently admitted patients
• Patient who can understand the purpose of the study and sign a consent form
• Patient has a measurable amount of edema
• Patient will likely be available during the time the clinicians can examine the patient

Exclusion Criteria

• Unable or unwilling to sign the consent form
• No measurable edema
• Currently in isolation for infection control purposes
• Patients in the Behavioral Health section of the hospital
• Maternity patients (due to availability of infant rooming-in)
• Prisoners
• Age below 18 years
• Patients with bilateral lower extremity amputation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Geisinger Clinic

OTHER

Sponsor Role: lead

Responsible Party

Richard Schreiber, MD FACP

Chief Medical Informatics Officer

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Richard Schreiber, MD

Role: PRINCIPAL_INVESTIGATOR

Geisinger Holy Spirit

Locations

Geisinger Holy Spirit

Camp Hill, Pennsylvania, United States

Countries

United States

Other Identifiers

2017-0434

Identifier Type: -

Identifier Source: org_study_id