Exploring the Outcomes and Financial Impact of a CBT-I Group Program Provided by Registered Nurses for Adults with Insomnia


  • Study type

  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 12-006921
    NCT ID: NCT02038556
    Sponsor Protocol Number: 12-006921

About this study

The purpose of this pilot study is to evaluate our RN CBT-I program outcomes and determine utility of this program as a high-value care model targeted specifically to our sleep center patient population.

Hypothesis: PIRS will improve from baseline to 2 month follow up

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria:

  • Able to speak english
  • Referred to Mayo Center for Sleep medicine Cognitive behaviorial therapy program for insomnia
  • no dementia

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Wendy Moore, M.S.N., R.N., N.E.-B.C.

Closed for enrollment

Contact information:

Wendy Moore M.S.N., R.N., N.E.-B.C.




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