Sleep for Optimal MEdical StudentS (PROMESS)

Determining the Influence of an Intervention Program Based on Sleep Improvement and Fatigue Reduction Among Medical Students.

Medical students have been shown to have a greater prevalence of poor sleep leading to poorer quality of life than other groups of students. Among medical students, poor sleep quality and insomnia have been associated with higher level of stress, as well as poorer academic performance. Our field surveys carried out in 2022 and 2023 at the Lyon Est medical school make the same alarming observation. They revealed that 53% of students had significant sleep problems.They also showed that students presented high levels of physical and mental fatigue. It is expected that these disorders will significantly degrade their quality of life as well as their health. Indeed, lack of sleep is associated with serious health problems such as illnesses cardiovascular or immune system deficiencies.

The PROMESS - SLEEP project aims to offer solutions to students to improve their sleep during their medical studies. It responds to a demand expressed by students: our field study showed that 40% of 4th year students declared being "very interested and/or interested" in following an intervention that aimed at improving sleep. An early knowledge of sleep optimization tools would allow students to quickly acquire the tools necessary to cope with the difficult conditions encountered during their training and lives of future doctors.The objective of this study is to determine the influence of an intervention program based on sleep improvement and fatigue reduction among medical students.

Study Overview

• Status: Recruiting
• Conditions: Fatigue; Sleep Disorder; Sleep; Health Behavior; Health-Related Behavior
• Intervention / Treatment: Behavioral: Sleep

Detailed Description

Our project aims to help future healthcare professionals to adopt health-promoting behaviors during their studies in a preventive approach. This support will be provided through an intervention program based on sleep improvement and fatigue reduction during their curriculum. Specifically, 4th and 5th-year students at the Faculty of Medicine of Lyon Est will have the opportunity to participate in the PROMESS SLEEP project. This intervention will span 11 weeks. At the end of this period, we expect improvements in both subjective and objective indicators of sleep and fatigue.

METHODS.

PRE-INTERVENTION. Week 1-3. Students will undergo a two-hour session, during which, they will complete questionnaires on sleep and fatigue. Then, they will wear actimeters to monitor sleep during three weeks.

INTERVENTION. From week 5 to week 11. The intervention will consist of three individual sessions, each lasting one hour, with approximately 15 days between each session. Each session includes individual interview between a sleep expert and the participant (i.e.student).The sessions will be scheduled as follow: week 5 and 6 (session 1), week 7 and 8 (session 2), week 9, 10, and 11 (session 3). During the interview, the expert will realize an initial assessment of student sleep and fatigue levels and will give personalized goals to student. Subsequent sessions follow the same structure.

• Study Type: Interventional
• Enrollment (Estimated): 45
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Sophie Schlatter, Dr.; Phone Number: 33 07 68 21 05 51; Email: sophie.schlatter@univ-lyon1.fr
• Study Contact Backup: Name: Angèle Métais, Dr.; Phone Number: 33 06 77 39 89 66; Email: angele.metais@univ-lyon1.fr

Study Locations

• France
  • Lyon, France, 69008
    • Recruiting
    • RESHAPE
    • Contact: Sophie Schlatter, Dr.; Phone Number: 33 07 68 21 05 51; Email: sophie.schlatter@univ-lyon1.fr
    • Contact: Angèle Métais, Dr.; Phone Number: 33 06 77 39 89 66; Email: angele.metais@univ-lyon1.fr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Being a 4th-year or a 5th-year medical student at the Faculty of Medicine Lyon East during the academic year 2023-2024.
• Having read the information note.
• Having signed the written consent.

Exclusion Criteria: No exclusion criteria will be applied.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Health Services Research
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Sleep intervention; One arm : All volunteers will receive a sleep management intervention.

Behavioral: Sleep; The sleep management intervention will consist of three individual sessions, each lasting one hour, with approximately 15 days between each session. The sessions will be scheduled as follow: week 5 and 6 (session 1), week 7 and 8 (session 2), week 9, 10, and 11 (session 3). During these sessions, subjective and objective indicators related to the sleep and fatigue levels will be recorded to assess the progress of each student.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Perceived level of sleep troubles. Evolution of the score obtained at the Pittsburgh Sleep Questionnaire Inventory (PSQI).	The students level of sleep troubles will be assessed through the PSQI score ranging from 0 (none) to 21 (extreme). This score classified the presence or absence of sleep troubles. It can be divided into eight sub-scores (i.e., sleep quality, sleep latency, time spent in bed, sleep time, habitual sleep efficiency, sleep disturbance, use of sleeping medication and daytime dysfunction). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Likert - expert satisfaction. Scores obtained on a Likert scale ranging from 1 to 5 accessing the expert's satisfaction of his/her intervention.	The perceived level of the expert satisfaction ("Are you satisfied with the session you just realized?") will be accessed on a likert scale ranging from 1 (not at all satisfied) to 5 (very satisfied). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
Likert - expert level of comfort. Score assessing the expert comfort levels in participant relationships on a likert scale ranging from 1 to 5.	The perceived level of expert comfort of the relationship with the student ("How comfortable did you feel with the student?") will be accessed on a likert scale ranging from 1 (not at all comfortable) to 5 (very comfortable). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
Likert - expert estimation of the overall student's achievements. Score obtained on a Likert scale ranging from 1 to 5 accessing the expert's level of satisfaction on the student's progress.	The level of expert satisfaction of the student's progress ("Are you satisfied with the student's progress during the all intervention?") will be accessed on a likert scale ranging from 1 (not at all satisfied) to 5 (very satisfied). This measure will be done at the session 3, i.e. approximately at week 9,11,10.	Week 9-10-11
Perceived level of sleep troubles. Score obtained at the Pittsburgh Sleep Questionnaire Inventory (PSQI).	The students basal level of sleep troubles will be assessed through the PSQI questionnaire ranging from 0 (none) to 21 (extreme). One score is assessed and classified the presence or absence of sleep troubles. It can be divided into eight sub-scores (i.e quality, latence, time spent in bed, sleep time, sleep efficacy, daytime dysfunction, sleep troubles and pills). This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Epworth Sleepiness scale. Score obtained at the Epworth Sleepiness scale.	The students basal level of diurnal sleepiness will be assessed through the Epworth Sleepiness scale ranging from 0 (none) to 24 (extreme). This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Multidimensional Fatigue. Score obtained at the Multidimensional Fatigue Inventory (MFI).	The students basal level of fatigue will be assessed through the MFI questionnaire that covers various dimensions of fatigue, including general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity; ranging from 4 to 20. A total score can also be assessed (from 20 to 100). This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Reduced composite scale of morningness. Score obtained at the reduced composite scale of morningness (RCSMS).	The students chronotype are assessed through the RCSMS. A total score can also be assessed (from 7 to 30). This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Time in Bed during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The time in bed (in hours/day) refers to the total duration between the time an individual gets into bed with the intention of sleeping and the time he/she get out of bed. It includes both the time spent asleep (total sleep time) and any periods of wakefulness while in bed. Essentially, it represents the total time allocated for sleep, regardless of whether the individual is actually sleeping during that time. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Total sleep duration during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings. The total duration of sleep is obtained during a specified period, measured in hours/day. It represents the overall quantity of sleep obtained by an individual.This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Sleep efficiency during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The sleep efficiency is the ratio of total sleep time to the total time spent in bed, expressed as a percentage. It reflects how effectively one is sleeping during the time allotted for sleep. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Sleep Onset Latency during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings. The sleep onset latency is the amount of time it takes for an individual to fall asleep after getting into bed, measured from the time the lights are turned off until sleep onset, reported in minutes.This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Wake after Sleep Onset during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The wake after sleep onset measures the total amount of time spent awake after initially falling asleep, reported in minutes. It reflects the disruptions in sleep continuity. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Number of Awakenings during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The number of awakenings represents the frequency of brief awakenings during the sleep period. Each awakening may disrupt the continuity of sleep and impact sleep quality. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Bedtime during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings. The bedtime is the time at which an individual goes to bed with the intention of sleeping. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Mid-sleep point during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The mid-sleep point refers to the midpoint of an individual's sleep period. It is calculated by finding the halfway point between the time of sleep onset (when the individual falls asleep) and the time of sleep offset (when the individual wakes up). This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Sleep Onset time during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The sleep onset time refers to the time at which an individual falls asleep after initially getting into bed with the intention of sleeping, measured in minutes.This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Sleep Inertia during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings. The sleep inertia refers to the periods between wake-up time and get-up time, measured in minutes. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Wake-up time during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings. The wake-up time refers to the time at which an individual awakens from sleep in the morning.This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Actimetry records. Sleep regularity index during the pre-intervention.	The objective students basal level of sleep will be accessed through the actimetry recordings.The sleep regularity index is a measure that evaluates the consistency of an individual's sleep habits over a given period. It takes into account the regularity of bedtime and wake-up times on a daily basis. The higher the sleep regularity index, the more consistent and regular the individual's sleep habits are considered to be. This measure will be done during the pre-interventional period at week 1.	Week 1 (Pre-intervention)
Multidimensional Fatigue. Evolution of the score obtained at the Multidimensional Fatigue Inventory (MFI) during the intervention.	The level of fatigue will be assessed through the MFI questionnaire that covers various dimensions of fatigue, including general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity; ranging from 4 to 20. A total score can also be assessed (from 20 to 100). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Time in Bed during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Total sleep duration during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Sleep efficiency during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Sleep Onset Latency during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Wake after Sleep Onset during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Number of Awakenings during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Mid-sleep point during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Bed time during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Sleep Onset Time during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Sleep Inertia during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Wake-up Time during the intervention.	The measure will be done between every session, i.e. between session 1 (week 5-6) and session 2 (week 7-8) and between session 2 and session 3 (week 9,10,11).	From week 5 to week 11.
Actimetry records. Evolution in Sleep regularity index during the intervention.	The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
VAS - sleep quantity: Evolution of the score obtained at the 100-mm Visual Analogue Scale (VAS) assessing the quantity of sleep.	The students level of sleep quantity will be assessed on a 100-mm Visual Analogue Scale (VAS: "Over the past two weeks, how would you characterize your sleep?") ranging from 0 (quantity of sleep largely insufficient) to 100 (quantity of sleep largely sufficient). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
VAS - sleep quality. Evolution of the score obtained at the 100-mm Visual Analogue Scale (VAS) characterizing the sleep quality.	The students sleep quality will be assessed on a 100-mm Visual Analogue Scale (VAS: "Over the past two weeks, how would you characterize your sleep?") ranging from 0 (the worst quality of sleep possible) to 100 (the best quality of sleep possible). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
VAS - sleep fatigue. Evolution of the score obtained at the 100-mm Visual Analogue Scale (VAS) assessing the perceived level of fatigue.	The students level of fatigue will be assessed on a 100-mm Visual Analogue Scale (VAS: "Over the past two weeks, how would you characterize your physical and mental fatigue levels?") ranging from 0 (extreme fatigue) to 100 (absence total of fatigue).The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
Advices given by the expert. Score obtained on a Likert scale ranging from 1 to 5 characterizing the nature of the advices given by the expert.	Following each session, the expert reported if he/she has given during the interview a specific advice according to apre-established list. For each pre-established advice, he/she has to report if : He/she didn't mention this; He/she mentioned this but didn't directly advise it; He/she mentioned this and recommended it; He/she had set this in the goals; The student was already doing it (positive reinforcement). The measure will be done every session, i.e. session 1 (week 5-6), session 2 (week 7-8) and session 3 (week 9,10,11).	From week 5 to week 11.
Likert - expert estimation of student's achievements. Score obtained on a Likert scale ranging from 1 to 3 accessing if the expert estimates that the student has achieve the goals previously set.	The expert evaluates, from 0 to 3 (i.e. 0 : not achieved at all, 1: slightly achieved, 2: fairly well achieved, 3: well achieved) if he/she estimates that the student has achieve the goals previously set. The measure will be done at session 2 (week 7-8) and session 3 (week 9,10,11).	From week 7 to week 11.
Composite score - Student's satisfaction. Score ranging from 0 to 100 accessing the student's level of satisfaction of the all intervention.	The composite score will be the mean of two sub-scores : An intervention specific score. Mean of the scores obtained at the two 100-mm Visual Analogue Scales ranging from 0 (absolutely not) to 100 (completely) :VAS: "Do you think the module has helped you to improve your sleep?"VAS: "Do you think the module has helped you to decrease your fatigue?"; An intervention general score. Mean of the scores obtained at the two 100-mm Visual Analogue Scales ranging from 0 (absolutely not) to 100 (completely) :VAS :"Do you think the proposed goals were suitable for your daily life?"VAS: "Do you think you can sustain the habit changes?" Theses measures will be done at the session 3, i.e. approximately at week 9,11,10.	Week 9-10-11

Collaborators and Investigators

• Sponsor: Research on Healthcare Performance Lab U1290
• Investigators: Principal Investigator: Sophie Schlatter, Dr., RESHAPE U1290 INSERM UCBL-LYON 1 Rockfeller, Lyon France.

Study record dates

Study Major Dates

• Study Start (Actual): November 11, 2023
• Primary Completion (Estimated): September 30, 2024
• Study Completion (Estimated): September 30, 2024

Study Registration Dates

• First Submitted: February 29, 2024
• First Submitted That Met QC Criteria: February 29, 2024
• First Posted (Actual): March 7, 2024

Study Record Updates

• Last Update Posted (Actual): March 7, 2024
• Last Update Submitted That Met QC Criteria: February 29, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Keywords: Fatigue; Sleep; Health; Student; Medical; Behaviour; Curriculum
• Additional Relevant MeSH Terms: Mental Disorders; Nervous System Diseases; Neurologic Manifestations; Fatigue; Sleep Wake Disorders
• Other Study ID Numbers: PROMESS - SLEEP

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No