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Clinical Trial Summary

Since psychiatry is still too often confronted with a dichotomy between psyche and soma, the assessment of pain and anxiety at RMI is still rarely done (Willer et al., 1982). The objective of this exploratory study is to evaluate the influence of pharmacological factors (type of injected molecules, injection frequency, injection site, treatment duration, treatment dose, time since last injection) and individual about the pain perceived when injecting antipsychotic therapy (diagnosis, sex, age, weight, duration of illness, level of anxiety, psychiatric and somatic comorbidity, insight). In the future, this study will develop a suitable procedure to limit pain and anxiety during RMI. Taking these dimensions into account will probably allow a better compliance of patients for this type of care, and thus a decrease in the number of relapses in the long term.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Delayed Antipsychotic Treatment, Pharmacological Factors and Individual Factors

NCT number NCT04784572
Study type Interventional
Source Centre hospitalier de Ville-Evrard, France
Contact Rusheenthira THAVASEELAN, MSC
Phone 0143093232
Email r.thavaseelan@epsve.fr
Status Recruiting
Phase N/A
Start date January 22, 2021
Completion date December 31, 2024