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A Study in Patients Reporting Cannabis Use Followed With an Application-Based Cannabis Journal (COSMIC- Releaf)

S

Scot Remick

Status

Not yet enrolling

Conditions

Cancer

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT07089225
5UG1CA189824 (U.S. NIH Grant/Contract)
20250219.1100

Details and patient eligibility

About

This study is being done because there is a significant lack of data on the use of cannabis amongst cancer patients. The investigators believe that the collection of this data will help researchers and clinicians better understand the needs and the impact of cannabis use in this specific patient population.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients must be 18 years of age or older and able to give verbal informed consent to participate.

  • Patients must be able to speak, read and understand English.

  • Patients must report use of cannabis at time of study participation.

  • Patients must have access to internet and ability to download Releaf™ App (MoreBetter, Ltd.) to a smartphone or tablet and must use Releaf™ App (MoreBetter, Ltd.) for cannabis journaling.

  • Patients must be able to send and receive text messages, and be able to interact with web-pages on smartphone or tablet.

  • There are 2 scenarios that patients are eligible for participation, and are listed below:

    1. Patients must have a cancer diagnosis for which they are receiving active therapy defined as follows:

      • Surgery - must be within a 30-day pre- and/or post-operative (peri-operative) window if single modality of care. Patients must be 18 years of age or older and able to give verbal informed consent to participate.
      • Radiation - must be within a 30-day pre- (simulation planning phase) and/or post-radiation window if single modality of care.
      • Any anticancer systemic therapy including hormonal, biologic, targeted, and/or cytotoxic chemotherapy. Understandably, numerous patients recruited under surgery and/or radiation will receive systemic therapy as part of combined modality therapy, which is permissible. Regardless, all details regarding cancer diagnosis, stage, and treatment will be collected from the EMR, which will be detailed in the informed consent document.
    2. Any patient in follow-up by their primary oncology care provider and/or AYA and cardio-oncology survivorship clinic(s).

  • All patients must be treated within the MHCCN thus ensuring access to clinical data in our system-wide EMR (Epic).

  • Patients must obtain their cannabis either from a medical-use store, adult-use (recreational) store or both. Patients must obtain cannabis ONLY from medical/recreational stores. Illicit (or homegrown) sources are strictly prohibited.

Trial contacts and locations

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Central trial contact

Clinical Research Coodinator; Research Program Manager

Data sourced from clinicaltrials.gov

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