environment-associated complaints
Conditions
Interventions
Group 1: Differences in individual disease models before and after biomonitoring of suspicious environmental novae.
The clinical trial consists of two patient contacts: First contact (first presentati
Sponsors
Universitätsklinikum FreiburgUni-Zentrum Naturheilkunde
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who visit an environmental university outpatient clinic for the first time and spontaneously (no active recruitment).
Exclusion criteria
Exclusion criteria: Pregnancy or lactation, relevant concomitant diseases such as heart failure, liver or kidney failure, tumor disease or a known psychiatric disease, known MCS, Sick-Building Syndrome or Chronic Fatigue Syndrome as well as anamnestically relevant environmental noxae
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Differences in the individual disease models of patients before and after biomonitoring of suspicious environmental novae. Primary outcome: Change in IPQ: Illness Perception Questionnaire, questionnaire on various dimensions of subjective disease models | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of personality structures, quality of life and psychological well-being of patients who change their disease model after biomonitoring with those who do not change their disease model | — |
Countries
Germany
Contacts
Public ContactClaudia Schultz
Institut für Umweltmedizin und Krankenhaushygiene
Outcome results
None listed