Effect of audiovisual Stimulation on Pruritus

Not Applicable

Recruiting

• Conditions: L29; L20; L28.2; L40; L98.9; Pruritus; Atopic dermatitis; Other prurigo; Psoriasis; Disorder of skin and subcutaneous tissue, unspecified

• Registration Number: DRKS00022374
• Lead Sponsor: niversitätsklinik für Dermatologie und Allergologie, Klinikum Oldenburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-08-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

patients with Atopic Dermatitis or Prurigo or other disease who suffer from intense Pruritus (NRS> 6)

Exclusion Criteria

Patients who cannot operate the video glasses on their own

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary endpoint is the intensity and quality of the patient's itch sensation. This is determined before, during and after the treatment using a questionnaire.

Secondary Outcome Measures

Name	Time	Method
Influence of the Pruritus quality and the type of disease on the intensity of the relief; Influence of age on the relief; Effect of audiovisual stimulation beyond the duration of the treatment