Efficacy and long-term effects of a specific dermatological rehabilitation program for patients with chronic pruritus

Efficacy and long-term effects of a specific dermatological rehabilitation program for patients with chronic pruritus - PruReha

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00032659

Enrollment

100

Registered

2023-09-28

Start date

2019-12-02

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

L29.9

Interventions

Group 1: Patients with chronic pruritus >6 weeks who have been admitted to a specific dermatological rehabiliation program will fill in the following patient-reported outcomes at admission, discharge,

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: chronic prurits >6 weeks

Exclusion criteria

Exclusion criteria: - exclusion of patients who are dependent on the sponsor/study director or the attending physician - patients identified as unfit to accurately and truthfully complete the questionnaires by the enrolling physician - patients who are not able to provide informed consent

Design outcomes

Secondary

Measure	Time frame
DLQI, GAD-7, PHQ-9, ItchyQoL, PBI, Subjective evaluation of therapeutic interventions and treatment outcome	—

Primary

Measure	Time frame
The long-term effects of a specific three-week dermatological rehabilitation program for patients with chronic pruritus (chronic pruritus > 6 weeks), measured with the numeric rating scale at admission, discharge, 4 week follow up and 12 week follow up after discharge.	—

Countries

Germany

Contacts

Public ContactAthanasios Tsianakas

Fachklinik Bad Bentheim

a.tsianakas@fk-bentheim.de(05922) 74-52 10

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026