Effect of audiovisual Stimulation on Pruritus

Effect of audiovisual Stimulation on Pruritus - ASOP

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00022374

Enrollment

150

Registered

2020-08-31

Start date

2020-08-10

Completion date

Unknown

Last updated

2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

L29 L20 L28.2 L40 L98.9

Interventions

Group 1: audiovisual Stimulation with videoglasses (HappyMed). Patients fill in a questionnaire describing the quality of their pruritus. Before, during and after the treastment patients rate their P

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Patients who cannot operate the video glasses on their own

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
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	—

Countries

Germany

Contacts

Public ContactMatthias Wilke

Universitätklinik für Dermatologie und Allergologie, Klinikum Oldenburg

Wilke.Matthias@klinikum-oldenburg.de+49 441 403 2851

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026