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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Wendy R. Moore, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT02038556
First received: June 10, 2013
Last updated: May 7, 2015
Last verified: May 2015
  Purpose

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


Condition Intervention
Insomnia Behavioral: cognitive behaviorial therapy -Insomnia

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Exploring the Outcomes and Financial Impact of a CBT-I Group Program Provided by Registered Nurses for Adults With Insomnia

Further study details as provided by Wendy R. Moore, Mayo Clinic:

Primary Outcome Measures:
  • Pittsburg insomnia rating scale [ Time Frame: up to 2 months ]

Enrollment: 60
Study Start Date: May 2013
Study Completion Date: September 2014
Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: cognitive behaviorial therapy for insomnia group program
Behavioral
Behavioral: cognitive behaviorial therapy -Insomnia

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
  • Able to speak english
  • Referred to Mayo Center for Sleep medicine Cognitive behaviorial therapy program for insomnia
  • no dementia
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02038556

Locations
United States, Minnesota
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Mayo Clinic
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Investigators
Principal Investigator: Wendy Moore, RN Mayo Clinic
  More Information

Responsible Party: Wendy R. Moore, Registered Nurse, Mayo Clinic
ClinicalTrials.gov Identifier: NCT02038556     History of Changes
Other Study ID Numbers: 12-006921
Study First Received: June 10, 2013
Last Updated: May 7, 2015

Additional relevant MeSH terms:
Sleep Initiation and Maintenance Disorders
Sleep Disorders, Intrinsic
Dyssomnias
Sleep Wake Disorders
Nervous System Diseases
Mental Disorders

ClinicalTrials.gov processed this record on September 21, 2017