Ignite Creation Date:
2024-05-06 @ 3:14 AM
Last Modification Date:
2024-10-26 @ 11:30 AM
Study NCT ID:
NCT02240082
Status:
UNKNOWN
Last Update Posted:
2015-10-27
First Post:
2014-09-10
Brief Title:
COPing With Shift Work - Web Based Program for Police Officers
Sponsor:
ISA Associates Inc
Organization:
ISA Associates Inc
Study Overview
Official Title:
COPing With Shift Work
Status:
UNKNOWN
Status Verified Date:
2015-10
Last Known Status:
ENROLLING_BY_INVITATION
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a clinical trial in which 300 Police Officers who currently work midnight shifts in the participating police departments will be recruited to test the effectiveness of a new web-based program to address sleep and associated problems related to shift work particularly night shift work Recruitment letters will be sent to all officers currently working midnight shift with the goal of recruiting 300 officers willing to participate in the study The 300 participants will be randomly assigned to either the experimental group receiving the web-based program or the waitlist control group Participants in the experimental group will be given access to the program site COPing with Shift Work and the mobile application Sleep Tracker Following completion of the field test participants in the control condition as well as all other interested officers will have access to the web-based COPing with Shift Work program
All participants will be asked to complete a baseline questionnaire containing multiple measures of sleep dietary practices physical activity and job performance Participants will be asked to complete the posttest approximately three months following initial access to the intervention
Primary and secondary outcome measures The Primary outcome measures are sleep quality as measured by the Pittsburgh Sleep Quality Index PSQI and sleepiness as measured by the sleepiness subscale of the widely used Karolinska Sleep Questionnaire KSQ The investigators have adapted the sleep measures to apply to individuals who work nights and may sleep during the day
Secondary outcome measures include the Nutritional Patterns Scale a 13-item modification of the Block Self-Administered Diet History Questionnaire assessing the nutritional value of the respondents diet Attitudes Toward a Healthy Diet a 17-item scale based on the Health Belief Model and developed and validated by Trenkner and associates assessing perceived benefits and barriers to eating a healthy diet the Godin Leisure-Time Exercise Questionnaire a brief 4-item query of usual leisure-time exercise habits and work productivity measured with the Work Limitations Questionnaire WLQ developed and validated by Lerner and associates
It is expected that the program group participants will have significantly better outcomes than the control group at three months
All participants will be asked to complete a baseline questionnaire containing multiple measures of sleep dietary practices physical activity and job performance Participants will be asked to complete the posttest approximately three months following initial access to the intervention
Primary and secondary outcome measures The Primary outcome measures are sleep quality as measured by the Pittsburgh Sleep Quality Index PSQI and sleepiness as measured by the sleepiness subscale of the widely used Karolinska Sleep Questionnaire KSQ The investigators have adapted the sleep measures to apply to individuals who work nights and may sleep during the day
Secondary outcome measures include the Nutritional Patterns Scale a 13-item modification of the Block Self-Administered Diet History Questionnaire assessing the nutritional value of the respondents diet Attitudes Toward a Healthy Diet a 17-item scale based on the Health Belief Model and developed and validated by Trenkner and associates assessing perceived benefits and barriers to eating a healthy diet the Godin Leisure-Time Exercise Questionnaire a brief 4-item query of usual leisure-time exercise habits and work productivity measured with the Work Limitations Questionnaire WLQ developed and validated by Lerner and associates
It is expected that the program group participants will have significantly better outcomes than the control group at three months
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 5R44HL114185 | NIH | None | httpsreporternihgovquickSearch5R44HL114185 |