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Real-World Observational Study on Patient-Reported Outcomes in the Treatment of Insomnia with Daridorexant in Canada

Insomnia

The purpose of this observational study is to evaluate the impact of daridorexant on quality of life, work productivity and insomnia symptoms in Canadian adults suffering from insomnia.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Signed ICF prior to any study-mandated procedure.
* Has received a first prescription of daridorexant 50 mg to treat insomnia, treatment start has not exceeded 7 days prior to enrollment.
* Ability to read and understand French or English.

Exclusion Criteria:

* Patients participating in a clinical trial.
* History of daridorexant use in the past (i.e., samples provided by the physician before prescription).
* Taking a concomitant medication to treat insomnia.
* Already started daridorexant more than 7 days prior to enrollment.The 7-day period is necessary to allow flexibility between the time of prescription and PROxy first contact to participant. Beyond this 7-day period, patients may already have experienced benefits from daridorexant. To minimize bias in baseline results, these patients will be excluded.

Study Location

PROxy Network, an initiative of PeriPharm inc.
PROxy Network, an initiative of PeriPharm inc.
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Jean Lachaine

[email protected]
514-731-8207
Study Sponsored By
PeriPharm
Participants Required
More Information
Study ID: NCT06311864