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Clinical Trials/NCT06342817
NCT06342817
Recruiting
Not Applicable

Effects of a Meditation Program on the Sleep Quality of Medicine Course Students

Universidade Federal da Fronteira Sul1 site in 1 country136 target enrollmentOctober 18, 2023
ConditionsSleep Disorder

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Disorder
Sponsor
Universidade Federal da Fronteira Sul
Enrollment
136
Locations
1
Primary Endpoint
Change in the quality of sleep of medical students on weeks 5, 9 and 17 by the PSQI and ESE
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The objective of the study is to evaluate the effect of an 8-week online mindfulness-based meditation program on quality sleep status of undergraduate students medicine in the city of Passo Fundo/RS and Chapecó/SC In addition to sleep quality, secondary outcomes such as mindfulness, symptoms of depression, stress, anxiety and burnout will also be assessed

Detailed Description

A controlled, single-center, randomized parallel group clinical trial will be developed to evaluate the effectiveness of an online mindfulness-based meditation program (POMBM) on the quality of sleep of medical students. The trial expects to involve 136 participants who will be randomized 1:1 into the intervention group or a waiting group (which will be called the control group), with 68 expected participants each. All trial procedures will take place online via Google meet and will consist of an invitation and presentation of the study, followed by an initial screening visit for those interested, and an intervention period of 8 weeks. The POMBM will be administered weekly online during the intervention period, with each session lasting 45 to 60 minutes. The control group will not perform any activities during the intervention period. Participants in both groups will be evaluated at the initial visit (T0), in the fifth week (T1), immediately after the end of the intervention period (T2) and in a 2-month follow-up after the end of the program (T3) using the following instruments : PSQI (Pittsburgh Quality Sleep Index), ESE (Epworth Sleepiness Scale), MAAS (Mindful Attention Awareness Scale), DASS-21 (Depression, Anxiety and Stress Scale), and CBI-S (Copenhagen Burnout Inventory Student Version)

Registry
clinicaltrials.gov
Start Date
October 18, 2023
End Date
June 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Universidade Federal da Fronteira Sul
Responsible Party
Principal Investigator
Principal Investigator

Tiago Teixeira Simon

Tiago Teixeira Simon

Universidade Federal da Fronteira Sul

Eligibility Criteria

Inclusion Criteria

  • Interest in participating in the study; over 18 years old; both genders; being duly registered in the Medicine course at Passo Fundo or Chapecó's faculties, from the 1st to 12th phase of the course

Exclusion Criteria

  • Have participated in another course or workshop on meditation in the last 4 weeks in addition to the invitation to study; being an active practitioner of meditation, yoga, tai-chi, qui-gong (at least 6 months before the start of the study); previous medical diagnosis of cognitive, language or communication deficits; alcohol dependence and other chemical substances; previous medical diagnosis of a disorder with risk of suicide or attempt of previous suicide; previous medical diagnosis of post-traumatic stress disorder; previous medical diagnosis of depressive disorder currently untreated; previous medical diagnosis of schizophrenia or delusional/hallucinatory disorders; previous medical diagnosis of social anxiety (difficulty being in a classroom)

Outcomes

Primary Outcomes

Change in the quality of sleep of medical students on weeks 5, 9 and 17 by the PSQI and ESE

Time Frame: week 0, week 5, week 9 and week 17

- PSQI (Pittsburgh Quality Sleep Index) - instrument consisting of 19 self-report questions categorized into seven components, graduated in scores from zero (no difficulty) to three (severe difficulty). The components of the PSQI are: C1 subjective sleep quality, C2 sleep latency, C3 sleep duration, C4 habitual sleep efficiency, C5 sleep changes, C6 use of sleeping medications C7 daytime sleep dysfunction. The sum of the values attributed to the seven components varies from zero to twenty-one in the total questionnaire score, indicating that the higher the number, the worse the sleep quality. A total score greater than five indicates that the individual is experiencing major dysfunction in at least two components, or moderate dysfunction in at least three components. ESE (Epworth Sleepiness Scale). This is a self-administered questionnaire that assesses the probability of falling asleep in eight situations involving daily activities, some of which are known to be highly soporific. The

Secondary Outcomes

  • Change in the awareness of medical students on weeks 5, 9 and 17 by the MAAS(week 0, week 5, week 9 and week 17)
  • Change in the burnout symptoms of medical students on weeks 5, 9 and 17 by CBI-S(week 0, week 5, week 9 and week 17)
  • Change in the depression, anxiety and stress symptoms of medical students on weeks 5, 9 and 17 by the DASS-21(week 0, week 5, week 9 and week 17)

Study Sites (1)

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