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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06436079
Other study ID # 44519 ANSIETAT UMH
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 6, 2024
Est. completion date December 2025

Study information

Verified date May 2024
Source Universitat de Girona
Contact Dalmau Vila-Vidal, MsC
Phone 972600160
Email dalmau.vila@udg.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this experimental study is to determine if the application of a nursing educational intervention reduces the anxiety of patients who are going to undergo treatment in the hyperbaric chamber. The researchers will compare the nursing educational intervention with the usual practice that is currently carried out in the unit for patients who are going to begin treatment in the hyperbaric chamber. Participants will: - Receive explanatory information through a camera triptych when the treatment is indicated. - Come half an hour before the first session to receive a nursing educational intervention, with audiovisual support, on the operation of the camera.


Description:

The objective of this experimental study is to determine if the application of a nursing educational intervention reduces the anxiety of patients who are going to undergo treatment in the hyperbaric chamber. An educational intervention will be applied to the intervention group that will begin on the same day that the treatment is indicated. That day, you will be given an informative brochure about the most important aspects you should know about the hyperbaric chamber. On the first day of the session, you will be asked to come half an hour early to explain, in more detail, what the hyperbaric chamber consists of and important aspects that you should take into account. The control group will receive the same intervention that is currently being carried out. Once treatment is prescribed in the chamber, they come on the first day and receive a brief explanation of how it works before entering.


Recruitment information / eligibility

Status Recruiting
Enrollment 42
Est. completion date December 2025
Est. primary completion date July 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Results in the Pfeiffer questionnaire<2. - That they understand Spanish or Catalan Exclusion Criteria: - That feel fear inside the hyperbaric chamber.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Intervention group
Patients who begin the first session in the hyperbaric chamber will receive a nursing educational intervention, with audiovisual support, about the operation of the chamber and aspects that must be taken into account once inside.

Locations

Country Name City State
Spain Hospital de Palamós Palamós Girona

Sponsors (1)

Lead Sponsor Collaborator
Universitat de Girona

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of anxiety measured with the STAI questionnaire. Feelings of fear, dread, and uneasiness that may occur as a reaction to stress. First week of treatment in the hyperbaric chamber
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