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Tailored cognitive-behavioral E-health care in patients with psoriasis.

Tailored cognitive-behavioral E-health care in patients with psoriasis.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25268
Enrollment
130
Registered
2010-07-30
Start date
2010-06-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Psoriasis

Interventions

Sponsors

Radboud University Nijmegen Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of definite psoriasis; 2. Age above 18 years.

Exclusion criteria

Exclusion criteria: 1. Pregnancy; 2. Illiteracy; 3. Severe physical and/or psychiatric comorbidity that interfere with the study protocol; 4. Current psychological treatments.

Design outcomes

Primary

MeasureTime frame
The primary outcome is the impact of psoriasis on daily life, including its impact on physical and psychological functioning and daily activities at post-treatment and follow-up measurement at 12 months. The primary outcome measures are measured as follows: 1. Impact on daily life: Composite scores of: A. Itch (IHDL, Evers et al., 2007); B. Fatigue (CIS, Vercoulen et al., 1994). 2. Impact on psychological functioning: Composite scores of: A. Negative mood (IHDL, Evers et al., 2007); B. Anxiety (IHDL, Evers et al., 2007); C. Depression (BDI, Beck et al., 1988). 3. Impact on daily activities: A. Role limitations due to emotional and physical health problems (SF-36, Ware et al., 1993).

Secondary

MeasureTime frame
Secondary outcomes include effects on disease severity as well as compliance with regular care and health care use.

Contacts

Public ContactA.W.M. Evers

LUMC PO Box 9555

a.evers@fsw.leidenuniv.nl+31 (0)71 527 3627

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)