SleepNCT07457476
Sleep Hygiene Education on the Sleep of Young Male Soccer Players
A study testing Sleep enhancement intervention in people with Sleep, run by João Barreira.
Trial summary
This will be a longitudinal study that aims to assess the effects of a sleep education and hygiene intervention on the sleep of young soccer players. The primary outcome of interest is the difference-in-differences in objectively measured sleep duration from baseline to post-intervention between the intervention and… Read more about this study
- Who is it for?
- Ages 16 to 19 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Sleep
- What is being tested?
- Sleep enhancement intervention
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 52 participants
- Where
- No sites listed yet
- Study dates
- 25 Feb 2026to 10 May 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 to 19 years
- Men only
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- Are actively playing soccer in the under-17 or under-19 of the soccer academy participating in the study.
- Are between 16 and 19 years old.
- Are available (i.e., no planned time off) during the monitoring period of the study.
Who cannot join
- Recent history of injury.
- In injury recovery process (i.e., return to play).
- Taking any medication that may impact sleep.
- Has travelled through multiple time zones in the past 3 months.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Effects of a Sleep Education and Hygiene Program on Sleep of Young High-level Male Soccer Players
This will be a longitudinal study that aims to assess the effects of a sleep education and hygiene intervention on the sleep of young soccer players.
The primary outcome of interest is the difference-in-differences in objectively measured sleep duration from baseline to post-intervention between the intervention and control groups.
Read the detailed description
METHODS Study Design This is an experimental study that aims to evaluate the impact of a sleep hygiene program on the sleep patterns of high-level adolescent male soccer players. Before the beginning of the study, subjects will fill out standardized sleep questionnaires. Then, subjects' sleep will be monitored using actigraphy and sleep diaries for 6 consecutive weeks (Weeks 1-2 Baseline; Weeks 3-4 Intervention; Weeks 5-6 Post-Intervention) and another 2 weeks, 6 weeks after the conclusion of the post-intervention period. The sleep diaries will be completed every morning, and information regarding bedtime and waketime will be combined with actigraphy data. After the baseline period, sleep data will be analyzed, and a tailored a sleep hygiene and education program will be built, tailored around the specific needs of the group of participants. At the same time, subjects will be randomly assigned to either control or intervention group.
Sample Size Calculation and Participant Recruitment Sample size was determined using simulation-based power analyses focused on the primary intervention effect, defined as the difference-in-differences (DiD) in sleep duration from baseline to post-intervention between the intervention and control groups. This effect reflects whether the change in sleep duration over time differs between groups and constitutes the primary outcome of interest. Although sleep was monitored across multiple periods, the power analysis focused on the pre-specified baseline to post-intervention contrast, as this corresponds to the primary causal effect of interest.
Expected effect sizes were informed by preliminary internal actigraphy data and recent sleep hygiene intervention literature. Specifically, the intervention group was expected to increase sleep duration by approximately 25 minutes from baseline to post-intervention, while the control group was expected to increase by approximately 5 minutes over the same period, resulting in an anticipated DiD of 20 minutes. Within-subject variability in sleep duration was estimated at 35-45 minutes and between-subject variability at 60-70 minutes, based on internal pilot data.
Power simulations were conducted assuming a 2 × 2 mixed design (group × time: pre- vs post-intervention), a common within-condition standard deviation of 35 minutes, and a within-subject correlation of 0.5. The required sample to achieve 80% power at an alpha level of 0.05, based on 2000 simulations runs using the ANOVA_power shiny app was tested. This was achieved using 50 participants (25 per group), with the group × time interaction corresponding to the DiD effect, for an approximate power of 81%.
Considering possible dropouts, missing data, available equipment and logistical constraints, 52 subjects will be recruited to participate in the study. According to the participant classification framework, recruited participants will be high-level male soccer players, competing in the Portuguese U17 and U19 national championship.
Written informed consent will be obtained prior to data collection from participants or their legal guardians (in case of participants younger than 18 years old). Pre-specified exclusion criteria included: having travelled across more than two time zones in the past three months, history of major injuries in the previous 3 months, prior history of a sleep-related disorder, and current medication that may interfere with sleep. The study will be conducted according to the Declaration of Helsinki and was approved by the Ethics Committee of the Portugal Football School (PFS 23/2023).
Randomization Participants were allocated to either the sleep hygiene intervention or control group using stratified block randomization. Stratification factors were sleep difficulty score (ASSQ categories) and sleep hygiene index (good, normal, poor). Within each stratum, participants were randomized in blocks of size 2 or 4 with a 1:1 allocation ratio. Random block sizes were used to reduce allocation predictability.
Sleep data analysis and program construction At the end of the baseline period, with the data gathered from the initial two weeks, the lead researcher will create a sleep education program, consisting of two 45-minute sessions delivered for a 2-week period (1 session per week) by the same specialist, and an individualized report containing each subjects' own sleep data (averaged and daily time in bed, sleep duration, sleep efficiency, bedtime, and waketime) and individualized recommendations. This report will be sent at the end of the intervention period. The recommendations will be centered at 1) improving time in bed and consequently increase sleep duration, 2) improving sleep schedules regularity and minimizing social jetlag, and 3) improving sleep hygiene behaviors reported through the Sleep Hygiene Index.
Sleep Education Sessions: The sessions will be designed to provide subjects with essential knowledge about sleep and its impact on performance and recovery, present strategies and behaviors (sleep hygiene) to improve sleep quantity and quality and tailored to each subject, considering the results of the Sleep Hygiene Index. In the space of two weeks, two 45-minutes sessions will be scheduled, one in the first week and another in the second week, and both will be given by the same specialist. The first session will address general sleep knowledge, including sleep stages, their benefits, sleep's role on athletic performance and recovery, and data from adolescents and adolescent athletes. The second session will be focused on sleep hygiene, discussing environmental factors such as light exposure, room temperature, and topics such as jet lag, sleep pressure, and technology's role on sleep.
Measures Sleep-related questionnaires At study onset, participants will complete five online self-administered questionnaires. These included the reduced Morningness-Eveningness Questionnaire (r-MEQ) for chronotype assessment, the Pittsburgh Sleep Quality Index (PSQI) for subjective sleep quality, the Epworth Sleepiness Scale (ESS) for perceived sleepiness, the Athlete Sleep Screening Questionnaire (ASSQ) for sleep difficulties and risk of sleep disturbances, and the Sleep Hygiene Index (SHI) to assess the practice of sleep hygiene behaviors. All questionnaires were completed prior to the main data collection period. After the post-intervention period, participants will complete the PSQI, ASSQ, ESS, and SHI again.
r-MEQ (Portuguese version): scores on the r-MEQ range from 4 to 25, and subjects are classified as morning-type (scores from 18-25), evening-type (scores from 12-17), or neither type (scores from 4-11).
PSQI: 19-item questionnaire organized into seven dimensions: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. A higher score indicates greater sleep disturbances, and the developers have suggested a cut- off score of 5 for the global scale to classify subjects with poor sleep quality.
ESS: total daytime sleepiness score ranges from 0-24 (0-7 normal, 8-9 mild excessive, 10-15 moderate excessive, and ≥ 16 severe excessive).
ASSQ: 15-item questionnaire that assesses sleep and circadian factors of sleep duration, sleep quality, symptoms of insomnia, and chronotype with a timeframe of "over the recent past". The sum of the first seven items comprises the sleep difficulty score (SDS) which is categorized into four intensities of the symptoms: none (0-4), mild (5-7), moderate (8-10), and severe (11-17).
SHI: 13-intem questionnaire used to assess habits and behaviors that affect sleep quality, with higher scores indicating poorer sleep hygiene. The questionnaire assesses topics such as regular sleep schedules, bedtime routine behaviors, and bedroom environment with the aim of identifying inadequate sleep practices that can be improved.
Sleep diaries Each morning and throughout the study period, participants will receive a daily link from the research staff and regular reminders from the club staff to maximize compliance. Each diary entry will include information regarding bedtime, wake-up time, and perceived fatigue, using the Rating-of-Fatigue scale. A researcher constantly checked data entries to monitor compliance and address missing data promptly.
Statistical Analysis Primary analysis The primary analysis will assess the intervention effect using a difference-in-differences approach, comparing changes in sleep duration from baseline to post-intervention between the intervention and control groups. This effect will be tested via the group × time interaction in a linear mixed-effects model.
Secondary analyses Secondary analyses will examine (i) difference-in-differences from baseline to the intervention period, (ii) within-group changes in sleep duration across periods, and (iii) longer-term follow-up effects. These analyses will be considered supportive and exploratory.
Statistical significance for the primary analysis will be defined as p < 0.05.
Missing data Linear mixed-effects models will be used to analyze sleep outcomes, allowing inclusion of all available data under a missing-at-random assumption. No imputation of missing sleep data is planned.
- Conditions
- Sleep
- Being tested
- Sleep enhancement intervention
- Keywords
- sleep education, recovery, sports, adolescent
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Sleep enhancement interventionBehavioural
Also called Sleep education, Sleep hygiene
Subjects will receive sleep education, sleep hygiene strategies, will have access to their sleep data and will have specific sleep objectives
| Study group | Role | What they receive |
|---|---|---|
| Control | No intervention | Subjects won't receive sleep education workshops and sleep data |
| Sleep Education | Experimental | Sbjects will receive sleep education and hygiene sessions, will receive their sleep data and will have objectives Receives: Behavioral: Sleep enhancement intervention |
What is being measured
The primary outcome is the main question the study is designed to answer.
Sleep duration
night sleep duration measured with objectively through wrist worn actigraphy devices
Measured: 6 weeks
Sleep efficiency
Sleep efficiency measured through wrist worn actigraphy devices. Sleep efficiency is one of the main sleep variables given through actigraphy sleep monitoring and one of the key proxies for sleep quality monitoring.
Measured: 6 weeks
Secondary outcomes (4)
Perceived fatigue
Perceived fatigue measures through the rating of fatigue scale (ROF). The rating of fatigue scale is a scale that measures perceived fatigue on a scale of 0 to 10. The higher the rating, the higher the fatigue. The ratings will be collected through an online forms that subjects have to fill daily, upon waking up.
Reminders to fill the forms will be sent out by a researcher enrolled in the project.
Measured: 6 weeks
Sleep/wake timings
bedtime and wake-up time, objectively measured through wrist worn actigraphy devices. Times are in h:min:ss format and are derived from the actigraphy devices.
Measured: 6 weeks
Athlete Sleep Screening Questionnaire.
15-item questionnaire that assesses sleep and circadian factors of sleep duration, sleep quality, symptoms of insomnia, and chronotype with a timeframe of "over the recent past" .The sum of the first seven items comprises the sleep difficulty score (SDS) which is categorized into four intensities of the symptoms: none (0-4), mild (5-7), moderate (8-10), and severe (11-17).
The questionnaire will be filled through an online forms.
Measured: At day one and in week 6
Sleep Hygiene Index
It is a 13-intem questionnaire used to assess habits and behaviors that affect sleep quality, with higher scores indicating poorer sleep hygiene. The questionnaire assesses topics of regular sleep schedules, bedtime routine behaviors, and bedroom environment with the aim of identifying inadequate sleep practices that can be improved. The final score is a sum of the 13 items, where each item has 4 options, scored from 0 to 4. The total final score, named the Sleep Hygiene Index, can range from 0 to 52. The higher the score, the worst sleep hygiene is classified.
Scoring Interpretation:
0-26: Good Sleep Hygiene 27-34: Moderate/Normal Sleep Hygiene 35+: Poor Sleep Hygiene
Measured: At day one and in week 6
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Mar 2026
- Study start25 Feb 2026 (estimated)
- Primary completion5 Apr 2026 (estimated)
- Study completion10 May 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SleepStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 52 participants (estimated)
Sponsor and investigators
- Lead sponsor
- João Barreira
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, João Barreira, University of Maia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07457476
- Sponsor's protocol ID
- phdjb05
- Status last verified
- Mar 2026
- First submitted
- 19 Feb 2026
- Last updated
- 11 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Data will be anonymized with each participant received a unique identifier code that only the responsible researcher will have access to. IPD data regarding the main study outcomes (sleep, perceptual measures, and sleep questionnaires) will be shared only with the core research team, if necessary, to discuss statistical analysis procedures.
Study at a glance
From the registry record, last updated by the sponsor on 11 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of a Sleep Education and Hygiene Program on Sleep of Young High-level Male Soccer Players
- ClinicalTrials.gov ID
- NCT07457476
- Acronym / sponsor ID
- phdjb05
- Conditions
- Sleep
- Keywords
- sleep education, recovery, sports, adolescent
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 52 participants (estimated)
- Lead sponsor
- João BarreiraUniversity, hospital or other
- Study start
- 25 Feb 2026 (estimated)
- Primary completion
- 5 Apr 2026 (estimated)
- Study completion
- 10 May 2026 (estimated)
- First posted
- 9 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This will be a longitudinal study that aims to assess the effects of a sleep education and hygiene intervention on the sleep of young soccer players.
The primary outcome of interest is the difference-in-differences in objectively measured sleep duration from baseline to post-intervention between the intervention and control groups.
Detailed description
METHODS Study Design This is an experimental study that aims to evaluate the impact of a sleep hygiene program on the sleep patterns of high-level adolescent male soccer players. Before the beginning of the study, subjects will fill out standardized sleep questionnaires. Then, subjects' sleep will be monitored using actigraphy and sleep diaries for 6 consecutive weeks (Weeks 1-2 Baseline; Weeks 3-4 Intervention; Weeks 5-6 Post-Intervention) and another 2 weeks, 6 weeks after the conclusion of the post-intervention period. The sleep diaries will be completed every morning, and information regarding bedtime and waketime will be combined with actigraphy data. After the baseline period, sleep data will be analyzed, and a tailored a sleep hygiene and education program will be built, tailored around the specific needs of the group of participants. At the same time, subjects will be randomly assigned to either control or intervention group.
Sample Size Calculation and Participant Recruitment Sample size was determined using simulation-based power analyses focused on the primary intervention effect, defined as the difference-in-differences (DiD) in sleep duration from baseline to post-intervention between the intervention and control groups. This effect reflects whether the change in sleep duration over time differs between groups and constitutes the primary outcome of interest. Although sleep was monitored across multiple periods, the power analysis focused on the pre-specified baseline to post-intervention contrast, as this corresponds to the primary causal effect of interest.
Expected effect sizes were informed by preliminary internal actigraphy data and recent sleep hygiene intervention literature. Specifically, the intervention group was expected to increase sleep duration by approximately 25 minutes from baseline to post-intervention, while the control group was expected to increase by approximately 5 minutes over the same period, resulting in an anticipated DiD of 20 minutes. Within-subject variability in sleep duration was estimated at 35-45 minutes and between-subject variability at 60-70 minutes, based on internal pilot data.
Power simulations were conducted assuming a 2 × 2 mixed design (group × time: pre- vs post-intervention), a common within-condition standard deviation of 35 minutes, and a within-subject correlation of 0.5. The required sample to achieve 80% power at an alpha level of 0.05, based on 2000 simulations runs using the ANOVA_power shiny app was tested. This was achieved using 50 participants (25 per group), with the group × time interaction corresponding to the DiD effect, for an approximate power of 81%.
Considering possible dropouts, missing data, available equipment and logistical constraints, 52 subjects will be recruited to participate in the study. According to the participant classification framework, recruited participants will be high-level male soccer players, competing in the Portuguese U17 and U19 national championship.
Written informed consent will be obtained prior to data collection from participants or their legal guardians (in case of participants younger than 18 years old). Pre-specified exclusion criteria included: having travelled across more than two time zones in the past three months, history of major injuries in the previous 3 months, prior history of a sleep-related disorder, and current medication that may interfere with sleep. The study will be conducted according to the Declaration of Helsinki and was approved by the Ethics Committee of the Portugal Football School (PFS 23/2023).
Randomization Participants were allocated to either the sleep hygiene intervention or control group using stratified block randomization. Stratification factors were sleep difficulty score (ASSQ categories) and sleep hygiene index (good, normal, poor). Within each stratum, participants were randomized in blocks of size 2 or 4 with a 1:1 allocation ratio. Random block sizes were used to reduce allocation predictability.
Sleep data analysis and program construction At the end of the baseline period, with the data gathered from the initial two weeks, the lead researcher will create a sleep education program, consisting of two 45-minute sessions delivered for a 2-week period (1 session per week) by the same specialist, and an individualized report containing each subjects' own sleep data (averaged and daily time in bed, sleep duration, sleep efficiency, bedtime, and waketime) and individualized recommendations. This report will be sent at the end of the intervention period. The recommendations will be centered at 1) improving time in bed and consequently increase sleep duration, 2) improving sleep schedules regularity and minimizing social jetlag, and 3) improving sleep hygiene behaviors reported through the Sleep Hygiene Index.
Sleep Education Sessions: The sessions will be designed to provide subjects with essential knowledge about sleep and its impact on performance and recovery, present strategies and behaviors (sleep hygiene) to improve sleep quantity and quality and tailored to each subject, considering the results of the Sleep Hygiene Index. In the space of two weeks, two 45-minutes sessions will be scheduled, one in the first week and another in the second week, and both will be given by the same specialist. The first session will address general sleep knowledge, including sleep stages, their benefits, sleep's role on athletic performance and recovery, and data from adolescents and adolescent athletes. The second session will be focused on sleep hygiene, discussing environmental factors such as light exposure, room temperature, and topics such as jet lag, sleep pressure, and technology's role on sleep.
Measures Sleep-related questionnaires At study onset, participants will complete five online self-administered questionnaires. These included the reduced Morningness-Eveningness Questionnaire (r-MEQ) for chronotype assessment, the Pittsburgh Sleep Quality Index (PSQI) for subjective sleep quality, the Epworth Sleepiness Scale (ESS) for perceived sleepiness, the Athlete Sleep Screening Questionnaire (ASSQ) for sleep difficulties and risk of sleep disturbances, and the Sleep Hygiene Index (SHI) to assess the practice of sleep hygiene behaviors. All questionnaires were completed prior to the main data collection period. After the post-intervention period, participants will complete the PSQI, ASSQ, ESS, and SHI again.
r-MEQ (Portuguese version): scores on the r-MEQ range from 4 to 25, and subjects are classified as morning-type (scores from 18-25), evening-type (scores from 12-17), or neither type (scores from 4-11).
PSQI: 19-item questionnaire organized into seven dimensions: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. A higher score indicates greater sleep disturbances, and the developers have suggested a cut- off score of 5 for the global scale to classify subjects with poor sleep quality.
ESS: total daytime sleepiness score ranges from 0-24 (0-7 normal, 8-9 mild excessive, 10-15 moderate excessive, and ≥ 16 severe excessive).
ASSQ: 15-item questionnaire that assesses sleep and circadian factors of sleep duration, sleep quality, symptoms of insomnia, and chronotype with a timeframe of "over the recent past". The sum of the first seven items comprises the sleep difficulty score (SDS) which is categorized into four intensities of the symptoms: none (0-4), mild (5-7), moderate (8-10), and severe (11-17).
SHI: 13-intem questionnaire used to assess habits and behaviors that affect sleep quality, with higher scores indicating poorer sleep hygiene. The questionnaire assesses topics such as regular sleep schedules, bedtime routine behaviors, and bedroom environment with the aim of identifying inadequate sleep practices that can be improved.
Sleep diaries Each morning and throughout the study period, participants will receive a daily link from the research staff and regular reminders from the club staff to maximize compliance. Each diary entry will include information regarding bedtime, wake-up time, and perceived fatigue, using the Rating-of-Fatigue scale. A researcher constantly checked data entries to monitor compliance and address missing data promptly.
Statistical Analysis Primary analysis The primary analysis will assess the intervention effect using a difference-in-differences approach, comparing changes in sleep duration from baseline to post-intervention between the intervention and control groups. This effect will be tested via the group × time interaction in a linear mixed-effects model.
Secondary analyses Secondary analyses will examine (i) difference-in-differences from baseline to the intervention period, (ii) within-group changes in sleep duration across periods, and (iii) longer-term follow-up effects. These analyses will be considered supportive and exploratory.
Statistical significance for the primary analysis will be defined as p < 0.05.
Missing data Linear mixed-effects models will be used to analyze sleep outcomes, allowing inclusion of all available data under a missing-at-random assumption. No imputation of missing sleep data is planned.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control | No intervention | –Subjects won't receive sleep education workshops and sleep data |
| Sleep Education | Experimental | Behavioral: Sleep enhancement interventionSbjects will receive sleep education and hygiene sessions, will receive their sleep data and will have objectives |
Who may qualify
- Ages
- 16 to 19 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (3 listed)
- Are actively playing soccer in the under-17 or under-19 of the soccer academy participating in the study.
- Are between 16 and 19 years old.
- Are available (i.e., no planned time off) during the monitoring period of the study.
Key exclusion criteria (4 listed)
- Recent history of injury.
- In injury recovery process (i.e., return to play).
- Taking any medication that may impact sleep.
- Has travelled through multiple time zones in the past 3 months.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Sleep enhancement interventionAlso: Sleep education, Sleep hygieneSubjects will receive sleep education, sleep hygiene strategies, will have access to their sleep data and will have specific sleep objectives | Behavioural | Sleep Education |
Primary outcome
Sleep duration
Time frame: 6 weeks
night sleep duration measured with objectively through wrist worn actigraphy devices
Sleep efficiency
Time frame: 6 weeks
Sleep efficiency measured through wrist worn actigraphy devices. Sleep efficiency is one of the main sleep variables given through actigraphy sleep monitoring and one of the key proxies for sleep quality monitoring.
4 secondary outcomes
Perceived fatigue
Time frame: 6 weeks
Sleep/wake timings
Time frame: 6 weeks
Athlete Sleep Screening Questionnaire.
Time frame: At day one and in week 6
Sleep Hygiene Index
Time frame: At day one and in week 6
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Mar 2026.
- Individual participant dataSharing planned: No. Data will be anonymized with each participant received a unique identifier code that only the responsible researcher will have access to. IPD data regarding the main study outcomes (sleep, perceptual measures, and sleep questionnaires) will be shared only with the core research team, if necessary, to discuss statistical analysis procedures.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A study testing Sleep enhancement intervention in people with Sleep, run by João Barreira.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 11 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact João Barreira, Master (+351 915941924, joao_barreira98@outlook.pt), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sleep duration (time frame: 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Mar 2026.