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NCT02038556 Clinical Trial

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

Insomnia Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02038556
Other study ID # 12-006921
Secondary ID
Status Completed
Phase N/A
First received June 10, 2013
Last updated May 7, 2015
Start date May 2013
Est. completion date September 2014

Study information
Verified date May 2015
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility - Able to speak english

- Referred to Mayo Center for Sleep medicine Cognitive behaviorial therapy program for insomnia

- no dementia

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• cognitive behaviorial therapy -Insomnia

Locations
Country Name City State
United States Mayo Clinic Rochester Minnesota
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pittsburg insomnia rating scale up to 2 months No
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