- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03014960
Effects of Leader Sleep Improvement on Leadership
October 24, 2017 updated by: Yu Tse Heng, University of Washington
The Effects of Leader Sleep Improvement on Leadership
The purpose of the study is to investigate the effects of sleep improvement in leaders on leader outcomes.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The investigators seek to extend the findings of a recent research which demonstrated that treating insomnia has several beneficial effects on employee work outcomes (Barnes, Miller, & Bostock, in press).
In the present study, the investigators propose that the treatment of leader insomnia would beneficially influence leadership, specifically abusive supervision, charismatic leadership, and laissez-faire leadership.
Study Type
Interventional
Enrollment (Anticipated)
400
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yu Tse Heng
- Phone Number: 412-517-2941
- Email: yutse@uw.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion criteria:
- Working adults who have at least one direct report (i.e., subordinate).
Exclusion criteria:
- Non-working adults/ adults who do not have at least one direct report (i.e., subordinate).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Experimental Condition
Online Cognitive Behavioral Therapy for Insomnia Intervention
|
CBT-I is a psychological treatment designed to break the patterns of maladaptive thinking and behavior that maintain insomnia.
CBT-I includes a range of techniques including a behavioral component (stimulus control, sleep restriction, relaxation) combined with a cognitive component (managing sleep related worries, the racing mind and intrusive thoughts) and an educational (sleep hygiene) component.
|
NO_INTERVENTION: Control Condition
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-Control Scale
Time Frame: 2 weeks
|
Rate self-control over the past 2 weeks.
Each item is scored 1-5 (1 = Very slightly or not at all, 2 = A little, 3 = Moderately, 4 = Quite a bit, 5 = Extremely).
|
2 weeks
|
Abusive Supervision Scale
Time Frame: 2 weeks
|
Rate abusive supervision over the past 2 weeks. Each item is scored 1-5:
|
2 weeks
|
Emotional Labor Scale
Time Frame: 2 weeks
|
Rate emotional labor over the past 2 weeks.
Each item is scored 1-5 (1 = Very slightly or not at all, 2 = A little, 3 = Moderately, 4 = Quite a bit, 5 = Extremely).
|
2 weeks
|
Charismatic Leadership Scale
Time Frame: 2 weeks
|
Rate charismatic leadership over the past 2 weeks.
Each item is scored 1-5 (1 = to a very little extent; 2 = to a little extent; 3 = to a moderate extent; 4 = to a great extent; 5 = to a very great extent).
|
2 weeks
|
Emotional Exhaustion Scale
Time Frame: 2 weeks
|
Rate emotional exhaustion over the past 2 weeks.
Each item is scored 1-5 (1 = Very slightly or not at all, 2 = A little, 3 = Moderately, 4 = Quite a bit, 5 = Extremely).
|
2 weeks
|
Laissez-Faire Leadership Scale
Time Frame: 2 weeks
|
Rate laissez-faire leadership over the past 2 weeks.
Each item is scored 1-5 (1 = to a very little extent; 2 = to a little extent; 3 = to a moderate extent; 4 = to a great extent; 5 = to a very great extent).
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Insomnia Scale
Time Frame: 2 weeks
|
Rate insomnia over the past 2 weeks.
Each item is scored 1-5 (1 = Very slightly or not at all, 2 = A little, 3 = Moderately, 4 = Quite a bit, 5 = Very much)
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yu Tse Heng, University of Washington
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
January 1, 2018
Primary Completion (ANTICIPATED)
June 1, 2018
Study Completion (ANTICIPATED)
June 1, 2018
Study Registration Dates
First Submitted
January 5, 2017
First Submitted That Met QC Criteria
January 6, 2017
First Posted (ESTIMATE)
January 9, 2017
Study Record Updates
Last Update Posted (ACTUAL)
October 26, 2017
Last Update Submitted That Met QC Criteria
October 24, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00000461-B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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