Ignite Creation Date:
2024-05-06 @ 8:23 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06364202
Status:
COMPLETED
Last Update Posted:
2024-04-15
First Post:
2024-04-09
Brief Title:
Effects of Peanut Butter on Sleep Quality and Daily Energy Levels in Fire Fighters
Sponsor:
Augusta University
Organization:
Augusta University
Study Overview
Official Title:
Effects of Peanut Butter on Sleep Quality and Daily Energy Levels in Fire Fighters
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
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:
The purpose of this study is to examine the possible benefits of peanut butter consumption prior to bedtime on sleep and energy levels among fire fighters Fire fighters require high levels of energy to perform their occupational tasks but commonly lack sleep as well as the amount of dietary protein and fat suggested for tactical athletes By addressing this gap we expect that if peanut butter consumption is shown to improve sleep andor energy this lifestyle change peanut butter consumption may be appealing to fire fighters because of the ease and low cost of peanut butter Aim 1 Determine if consuming peanut butter prior to bedtime alters measures of sleep quality and quantity in fire fighters It is hypothesized that firefighters who consume the peanut butter will have positive impacts in measure of sleep quality and energy levels
Aim 2 Examine the effects of peanut butter consumption on morning and evening energy levels
Aim 2 Examine the effects of peanut butter consumption on morning and evening energy levels
Detailed Description:
This study will utilize a randomized parallel-arm placebo-controlled design to determine the impact peanut butter consumption may have on sleep and energy levels in firefighters when consumed before bed-time Forty local fire fighters will be recruited to complete this eight-week study week one will constitute a baseline and weeks 2-8 will consist of the intervention A blinded statistician will randomize the participants into one of two groups a control group and a peanut butter group During the first familiarization visit all participants will sign an informed consent receive height and weight measurements waist and hip circumference measurements blood pressure measurement fill out a 30-day diet recall fill out 3 questionnaires Insomnia Severity Index PTSD-checklist 5 PCL-5 and Dispositional Resilience will take 10 minutes to fill out and receive a validated sleep monitor Actigraph GT3X watch and heart rate monitor chest strap and 14 Visual Analogue Scale VAS questionnaires which assess energy levels and time of last caffeine alcohol and screen time before bed They will wear the watch for seven days along with the heart rate monitor for 5 nights and complete the VAS twice a day for seven days on qualtrics while maintaining a normal diet and physical activity A link to take the surveys will be provided during the familiarization visit After this baseline week participants will then continue to wear the Actigraph watch daily for seven weeks and fill out a VAS twice a day while taking part in their specified intervention Those in the control group will proceed with the same protocol as for the baseline week Those in the peanut butter group will also continue with the same protocol as in the baseline week with the addition of consuming two tablespoons of peanut butter two hours before bed for five nights a week during the seven-week intervention We will provide a tablespoon measurer and three jars of natural peanut butter to the participants in the peanut butter group To increase ease of participation we will meet in a private room at the local fire stations to collect data Both the peanut butter and control group will be asked not to eat anything two hours before bed during those five days after the peanut butter serving in the peanut butter group The peanut butter consumption is dependent on randomization group assignment Participants in both groups will be asked to maintain their normal diet and not change their physical activity levels andor begin a weight loss program throughout their time in the study approximately eight-weeks
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None