Psychoeducational Intervention for Sleep Health in University Students
Sleep health education
Sleep Hygiene+6
+ Treatment Adherence and Compliance
+ Adherence Interventions
Prevention Study
Summary
Study start date: February 1, 2024
Actual date on which the first participant was enrolled.This study focuses on understanding and improving sleep health among university students through a psychoeducational intervention. It aims to identify the psychological and social factors affecting students' sleep and to implement an intervention that could potentially enhance their sleep quality. University students often face challenges with maintaining healthy sleep due to academic pressures and lifestyle habits. By exploring these factors, the study seeks to develop effective strategies to prevent sleep issues and promote better sleep health, which is crucial for students' overall well-being and academic performance. Participants in this study will undergo a three-week psychoeducational program designed to improve their sleep habits. This program includes various sessions, which are conducted face-to-face, facilitated by trained instructors, and supported by teaching materials like manuals. The study evaluates how well participants understand and follow the program, as well as the practicality of the sessions, including the venue, group size, and length of sessions. While the main focus is not directly on measuring specific outcomes, the feedback collected will help refine and enhance the intervention for future use, ensuring it is accessible and relevant to the students' needs.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.92 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 30 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Centre d'études des troubles du sommeil (CETS)
Québec, CanadaOpen Centre d'études des troubles du sommeil (CETS) in Google Maps