蹤獲扦

Skip to main content

Does a Virtual Coach Offer a Better Solution for Weight Reduction in Ventral Hernia Patients with Obesity?

  • Status
    Accepting Candidates
  • Age
    18 Years - 90 Years
  • Sexes
    All
  • Healthy Volunteers
I'm interested
Share this study

Description

This research is to use a virtual coach to assist hernia patients overcome the difficulties that prevent weight loss before having ventral hernia surgery.  We aim to conduct a two-arm, pragmatic clinical trial that compares the use of the integrated virtual coach to standard of care on preoperative weight loss for hernia repair patients.

Details

Protocol number 202300391

Eligibility

Inclusion criteria:

Patients 18 years of age and older with a Body Mass Index (BMI) of 30 and above and diagnosed with Obesity by the ICD 10 Code: E66.9 who have been evaluated by a surgeon and offered elective ventral hernia repair Also, have a complete medical record that allows for statistical calculations to be performed. 

Exclusion criteria:

Pregnant females, patients with severe mental disorders, prescribed psychiatric medications associated with weight gain, a history of a Substance Use Disorder, patients on long-term steroid therapy, and patients with insufficient medical records.

Participate in a study

Here are some general steps to consider when participating in a research study:

  1. Step
    1

    Contact the research team

    Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.

    Primary contact

  2. Step
    2

    Get screened to confirm eligibility

    You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.

  3. Step
    3

    Provide your consent to participate

    If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.

  4. Step
    4

    Participate

    If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.