Drinking, AlcoholBEER-HIITNCT03660579
Beer or Ethanol Effects on the Response to High Intensity Interval Training: A Controlled Study in Healthy Individuals
A study testing HIIT-AB Group, HIIT-NAB Group and HIIT-SW Group in people with Drinking, Alcohol and Exercise, run by Universidad de Granada at 1 site in Spain.
Trial summary
HIIT-BEER will determine the effect of habitual and moderate beer intake (330-660 ml / day, 5 days / week) on physical fitness, body composition, psychokinetic abilities and psychological status in sedentary healthy adults undergoing a HIIT training program. Read more about this study
- Who is it for?
- Ages 18 to 40 yearsHealthy volunteers can take part
- Conditions the study is for
- Drinking, Alcohol, Exercise
- What is being tested?
- HIIT-AB Group, HIIT-NAB Group and HIIT-SW Group
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteSpain
- Study dates
- 20 Jan 2018to 1 Jun 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 18 to 40 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Age: 18-40 years
- BMI:18.5-25 kg/m2
- Not engaged in regular physical activity >20min on >3days/week
- Not participating in a weight loss programme
- Stable weight over the last 5 months (body weight changes>5kg)
- Participant must be capable and willing to provide consent, understand exclusion criteria and accept the randomized group assignment
- Normal electrocardiogram
- Not personal family history related to alcohol consumption.
Who cannot join
- History of cardiovascular disease
- Diabetes
- Pregnancy or planning to get pregnant during study period
- Beta blockers or benzodiapezins use
- Taking medication for thyroid
- Other significant conditions that are life-threatening or that can interfere with or be aggravated by exercise
- Unwillingness to either complete the study requirements or to be randomized into control or training group
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Beer or Ethanol Effects on the Response to High Intensity Interval Training: A Controlled Study in Healthy Individuals: BEER - HIIT Study
HIIT-BEER will determine the effect of habitual and moderate beer intake (330-660 ml / day, 5 days / week) on physical fitness, body composition, psychokinetic abilities and psychological status in sedentary healthy adults undergoing a HIIT training program.
Read the detailed description
Aims:
To determine the effect of habitual and moderate consumption of beer on physical fitness, body composition, psychokinetic and cognitive abilities and psychological status in sedentary healthy adults undergoing a HIIT training program.
The primary hypothesis will that a HIIT program will induce an improvement on physical fitness, body composition, psychokinetic abilities and psychological responses compared to a control group but this positive effect could be blunted by alcohol intake.
Methods:
HIIT-BEER will recruit 80 sedentary, healthy, adults (50% women) aged 18-40 years.
Will be performed a 10-week controlled trial in which the effects of HIIT will be compared to a control group without training. The effects of habitual intake of different alcoholic beverage will be also compared.
After completing the baseline measurements, the selected participants will be randomly assigned to either the control or the exercise training groups. The participants included in the training groups will be asked to choose individual choice about their drinking preference for alcoholic or non-alcoholic beverages. The participants who chose alcohol intake will be randomly assigned into the training group with alcohol beer intake (5.4% Alcohol-Special Alhambra®, Cervezas Alhambra, Spain) or to the sparkling water group with exactly the same amount of distilled alcohol added. The distilled alcoholic beverage used for the investigator's study will be vodka because of the purity of its composition (37.5% ethanol and 62.5% water). The participants who chose non-alcoholic beverages will be randomized into the training groups of non-alcohol beer (0.0% alcohol-Cruzcampo®, Heineken España) or sparkling water (Eliges (IFA) Eliqua 2®, Font Salem, Spain) intakes.
So, eligible participants will be assigned to five groups: (i) a group that will performed HIIT and will consumed 330 ml (women) or 2x300 ml (men) of beer with 5.4% alcohol (HIIT-AB, n=16); (ii) a group that will performed HIIT and will consumed the same amount of beer without alcohol (0.0%) (HIIT-NAB; n=16); (iii) a group that will performed HIIT and will consumed the same amount of sparkling water (0.0%) (HIIT-W; n=16); (iv) a group that will performed HIIT and will consumed sparkling water with the same amount of alcohol than the pre-established beer (5.4%) (HIIT-ASW; n=16); and (v) a control group that will not perform any physical training program (CON; n=16).
The beverage intakes will be programmed from Monday to Friday. There will not specific recommendation for Saturday and Sunday, but the participants will be instructed to keep a moderate alcohol during the weekend.
Laboratory measures completed at baseline and 10 weeks later, include physical fitness (cardiorespiratory fitness, muscular strength), body composition, hearth rate variability (HRV), reaction time, cognitive variables and health-related questionnaires. The investigators will also obtain dietary habits data and cardiovascular disease risk factors.
- Conditions
- Drinking, Alcohol, Exercise
- Being tested
- HIIT-AB Group, HIIT-NAB Group, HIIT-SW Group, HIIT-ASW Group
- Keywords
- Physical fitness, Recovery, Stress, Training, HIIT, Beer
- Medical subject headings
- Alcohol Drinking, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HIIT-AB GroupOther
Group that performed HIIT and consumed 330 ml (women) or 2x300 ml (men) of beer with 5.4% alcohol.
HIIT-NAB GroupOther
Group that performed HIIT and consumed 330 ml (women) or 2x300 ml (men) of beer without alcohol (0.0%).
HIIT-SW GroupOther
Group that performed HIIT and consumed the same amount of sparkling water (0.0%).
HIIT-ASW GroupOther
Group that performed HIIT and consumed sparkling water with the same amount of alcohol than the pre-established beer (5.4%).
| Study group | Role | What they receive |
|---|---|---|
| HIIT-CON | No intervention | No intervention: Control |
| HIIT-AB Group | Experimental | Intake:
330ml (women) or 2x300 ml (men) of beer with 5.4% alcohol. The beverage intakes will be programmed from Monday to Friday.
Training:
The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale).
All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. Receives: Other: HIIT-AB Group |
| HIIT-NAB Group | Experimental | Intake:
330 ml (women) or 2x300 ml (men) of beer without alcohol (0.0%). The beverage intakes will be programmed from Monday to Friday.
Training:
The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale).
All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. Receives: Other: HIIT-NAB Group |
| HIIT-SW Group | Experimental | Intake:
330 ml (women) or 2x300 ml (men) of sparkling water. The beverage intakes will be programmed from Monday to Friday.
Training:
The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale).
All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. Receives: Other: HIIT-SW Group |
| HIIT-ASW Group | Experimental | Intake:
330 ml (women) or 2x300 ml (men) of sparkling water with 5.4% alcohol.The beverage intakes will be programmed from Monday to Friday.
Training:
The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale).
All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. Receives: Other: HIIT-ASW Group |
What is being measured
The primary outcome is the main question the study is designed to answer.
Physical Fitness Cardiorespiratory fitness
Cardiorespiratory fitness measure through a maximum treadmill test (VO2 max.).
Measured: Baseline and through study completion, an average of 10 weeks.
Secondary outcomes (18)
Physical Fitness: Muscular strength (Bosco Test)
Muscle strength measure through: Bosco test.
Measured: Baseline and through study completion, an average of 10 weeks.
Physical Fitness: Muscular strength (Handgrip strength)
Muscle strength measure through: Handgrip strength.
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (DXA)
Body composition measure through: Dual-energy X-ray absorptiometry (DXA).
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (Weight)
Body composition measure through: Anthropometry (Weight in kg).
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (Height)
Body composition measure through: Anthropometry (Height in meter).
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (Hip perimeter)
Body composition measure through: Anthropometry (Hip perimeter in cm)
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (Waist circumference)
Body composition measure through: Anthropometry (Waist circumference in cm).
Measured: Baseline and through study completion, an average of 10 weeks.
Body composition (Neck perimeter)
Body composition measure through: Anthropometry (Neck perimeter in cm).
Measured: Baseline and through study completion, an average of 10 weeks.
Heart Rate Variability
Measure by Polar RS800CX.
Measured: Baseline and through study completion, an average of 10 weeks.
Reaction time
Measure by Vienna Test System.
Measured: Baseline and through study completion, an average of 10 weeks.
Memory
Measure by Spanish-Complutense Verbal Learning Test (TAVEC)
Measured: Baseline and through study completion, an average of 10 weeks.
Attention
Measure by D2 Test.
Measured: Baseline and through study completion, an average of 10 weeks.
Working Memory
Measure by Numbers and Letters (WISC-IV).
Measured: Baseline and through study completion, an average of 10 weeks.
Verbal fluency
Verbal fluency assessment test.
Measured: Baseline and through study completion, an average of 10 weeks.
Questionnaires and Scales
Measure by:
- PREDIMED Questionnaire on Adherence to the Mediterranean Diet.
- Beverage Intake Questionnaire (PREDIMED).
- Questionnaire of the Five Great Factors of the Personality (BFQ).
- Satisfaction with life (SWL).
- Health questionnaire (SF-36).
- International Fitness Scale Questionnaire (IFIS).
- Beck Depression Inventory (BDI-II).
- Life Orientation test questionnaire (LOT-R).
- Sexual desire questionnaire.
- Sexual functioning questionnaire.
- Pittsburgh Sleep Quality Index.
- Profile of Mood States Questionnaire (POMS).
- Scale of Subjective Happiness.
- Emotional Intelligence Scale (TMMS).
- Scale Panas of positive and negative affect.
- Perceived stress scale (PSS).
- Scale of assessment of mood (EVEA).
- Eating habits questionnaire.
- Spanish versión of Three Factor EatingQuestionnaire-R18 (TFEQ-SP)
- Scale of regulation of the behavior in physical exercise (BREQ-2).
- Scale of measurement of the orientations of goals in the exercise (GOES)
Measured: Baseline and through study completion, an average of 10 weeks.
Questionnaires and Scales
Measure by:
(BDI-II); PREDIMED Questionnaire on Adherence to the Mediterranean Diet ; Sexual desire questionnaire; Sexual functioning questionnaire; Eating habits questionnaire; Beverage Intake Questionnaire (PREDIMED); Perceived stress scale (PSS); Scale of Subjective Happiness; EVEA; IFIS; Pittsburgh Sleep Quality Index; BFQ; LOT-R; PANNAS; POMS; SWLS; TMMS-24 and TFEQ-SP.
Measured: Every week
Questionaires and Scales
Measure by:
PSS; EVEA; PANNAS; TMMS-24
Measured: Every two weeks
Questionnaires and Scales
Measure by:
Scale of Subjective Happiness; Pittsburgh Sleep Quality Index; POMS; BREQ-2 and GOES.
Measured: Every three weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Sep 2018
- Study start20 Jan 2018
- Primary completion20 May 2018
- Study completion1 Jun 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Drinking, AlcoholStudies 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
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universidad de Granada
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Manuel Castillo Garzón, Universidad de Granada
- Investigators
- Manuel J. Castillo Garzón, Principal investigator, Universidad de Granada
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03660579
- Sponsor's protocol ID
- 321/CEIH/2017
- Acronym
- BEER-HIIT
- Status last verified
- Sep 2018
- First submitted
- 20 Jul 2018
- Last updated
- 6 Sep 2018
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Navarro-Lomas G, De-la-O A, Dote-Montero M, Castillo MJ, Amaro-Gahete FJ, Plaza-Florido A. Moderate alcohol intake and heart rate variability adaptations to high-intensity interval training in healthy young adults: the BEER-HIIT study. Front Cardiovasc Med. 2026 Aug 25;13:1920023. doi: 10.3389/fcvm.2026.1920023. eCollection 2026.
PubMed 42712702Molina-Hidalgo C, De-la-O A, Dote-Montero M, Amaro-Gahete FJ, Castillo MJ. Influence of daily beer or ethanol consumption on physical fitness in response to a high-intensity interval training program. The BEER-HIIT study. J Int Soc Sports Nutr. 2020 May 27;17(1):29. doi: 10.1186/s12970-020-00356-7.
PubMed 32460793
Study at a glance
From the registry record, last updated by the sponsor on 6 Sep 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Beer or Ethanol Effects on the Response to High Intensity Interval Training: A Controlled Study in Healthy Individuals: BEER - HIIT Study
- ClinicalTrials.gov ID
- NCT03660579
- Acronym / sponsor ID
- BEER-HIIT / 321/CEIH/2017
- Conditions
- Drinking, Alcohol, Exercise
- Keywords
- Physical fitness, Recovery, Stress, Training, HIIT, Beer
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Universidad de GranadaUniversity, hospital or other
- Study start
- 20 Jan 2018 (actual)
- Primary completion
- 20 May 2018 (actual)
- Study completion
- 1 Jun 2018 (actual)
- First posted
- 6 Sep 2018 (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.
HIIT-BEER will determine the effect of habitual and moderate beer intake (330-660 ml / day, 5 days / week) on physical fitness, body composition, psychokinetic abilities and psychological status in sedentary healthy adults undergoing a HIIT training program.
Detailed description
Aims:
To determine the effect of habitual and moderate consumption of beer on physical fitness, body composition, psychokinetic and cognitive abilities and psychological status in sedentary healthy adults undergoing a HIIT training program.
The primary hypothesis will that a HIIT program will induce an improvement on physical fitness, body composition, psychokinetic abilities and psychological responses compared to a control group but this positive effect could be blunted by alcohol intake.
Methods:
HIIT-BEER will recruit 80 sedentary, healthy, adults (50% women) aged 18-40 years.
Will be performed a 10-week controlled trial in which the effects of HIIT will be compared to a control group without training. The effects of habitual intake of different alcoholic beverage will be also compared.
After completing the baseline measurements, the selected participants will be randomly assigned to either the control or the exercise training groups. The participants included in the training groups will be asked to choose individual choice about their drinking preference for alcoholic or non-alcoholic beverages. The participants who chose alcohol intake will be randomly assigned into the training group with alcohol beer intake (5.4% Alcohol-Special Alhambra®, Cervezas Alhambra, Spain) or to the sparkling water group with exactly the same amount of distilled alcohol added. The distilled alcoholic beverage used for the investigator's study will be vodka because of the purity of its composition (37.5% ethanol and 62.5% water). The participants who chose non-alcoholic beverages will be randomized into the training groups of non-alcohol beer (0.0% alcohol-Cruzcampo®, Heineken España) or sparkling water (Eliges (IFA) Eliqua 2®, Font Salem, Spain) intakes.
So, eligible participants will be assigned to five groups: (i) a group that will performed HIIT and will consumed 330 ml (women) or 2x300 ml (men) of beer with 5.4% alcohol (HIIT-AB, n=16); (ii) a group that will performed HIIT and will consumed the same amount of beer without alcohol (0.0%) (HIIT-NAB; n=16); (iii) a group that will performed HIIT and will consumed the same amount of sparkling water (0.0%) (HIIT-W; n=16); (iv) a group that will performed HIIT and will consumed sparkling water with the same amount of alcohol than the pre-established beer (5.4%) (HIIT-ASW; n=16); and (v) a control group that will not perform any physical training program (CON; n=16).
The beverage intakes will be programmed from Monday to Friday. There will not specific recommendation for Saturday and Sunday, but the participants will be instructed to keep a moderate alcohol during the weekend.
Laboratory measures completed at baseline and 10 weeks later, include physical fitness (cardiorespiratory fitness, muscular strength), body composition, hearth rate variability (HRV), reaction time, cognitive variables and health-related questionnaires. The investigators will also obtain dietary habits data and cardiovascular disease risk factors.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| HIIT-CON | No intervention | –No intervention: Control |
| HIIT-AB Group | Experimental | Other: HIIT-AB GroupIntake: 330ml (women) or 2x300 ml (men) of beer with 5.4% alcohol. The beverage intakes will be programmed from Monday to Friday. Training: The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale). All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. |
| HIIT-NAB Group | Experimental | Other: HIIT-NAB GroupIntake: 330 ml (women) or 2x300 ml (men) of beer without alcohol (0.0%). The beverage intakes will be programmed from Monday to Friday. Training: The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale). All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. |
| HIIT-SW Group | Experimental | Other: HIIT-SW GroupIntake: 330 ml (women) or 2x300 ml (men) of sparkling water. The beverage intakes will be programmed from Monday to Friday. Training: The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale). All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. |
| HIIT-ASW Group | Experimental | Other: HIIT-ASW GroupIntake: 330 ml (women) or 2x300 ml (men) of sparkling water with 5.4% alcohol.The beverage intakes will be programmed from Monday to Friday. Training: The volume in HIIT 40-65 min/week at high intensity. HIIT with short intervals. Frequency two times/week. Load variation. Gradual progression to control the exercise dose. Periodization divided in: familiarization phase, phase I, phase II. Sessions. The participants will performed 8 weight-bearing exercises (in circuit form) 2 times/set with an active rest (walking at 6 RPE scale) as many times at as defined. The HIIT intensity will controlled by RPE (0-10 RPE scale). All sessions will be started with a dynamic standardized warm-up, including several muscle activation exercises, and will be ended with a cooling-down protocol. |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (8 listed)
- Age: 18-40 years
- BMI:18.5-25 kg/m2
- Not engaged in regular physical activity >20min on >3days/week
- Not participating in a weight loss programme
- Stable weight over the last 5 months (body weight changes>5kg)
Key exclusion criteria (7 listed)
- History of cardiovascular disease
- Diabetes
- Pregnancy or planning to get pregnant during study period
- Beta blockers or benzodiapezins use
- Taking medication for thyroid
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 |
|---|---|---|
| HIIT-AB GroupGroup that performed HIIT and consumed 330 ml (women) or 2x300 ml (men) of beer with 5.4% alcohol. | Other | HIIT-AB Group |
| HIIT-NAB GroupGroup that performed HIIT and consumed 330 ml (women) or 2x300 ml (men) of beer without alcohol (0.0%). | Other | HIIT-NAB Group |
| HIIT-SW GroupGroup that performed HIIT and consumed the same amount of sparkling water (0.0%). | Other | HIIT-SW Group |
| HIIT-ASW GroupGroup that performed HIIT and consumed sparkling water with the same amount of alcohol than the pre-established beer (5.4%). | Other | HIIT-ASW Group |
Primary outcome
Physical Fitness Cardiorespiratory fitness
Time frame: Baseline and through study completion, an average of 10 weeks.
Cardiorespiratory fitness measure through a maximum treadmill test (VO2 max.).
18 secondary outcomes
Physical Fitness: Muscular strength (Bosco Test)
Time frame: Baseline and through study completion, an average of 10 weeks.
Physical Fitness: Muscular strength (Handgrip strength)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (DXA)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (Weight)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (Height)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (Hip perimeter)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (Waist circumference)
Time frame: Baseline and through study completion, an average of 10 weeks.
Body composition (Neck perimeter)
Time frame: Baseline and through study completion, an average of 10 weeks.
Heart Rate Variability
Time frame: Baseline and through study completion, an average of 10 weeks.
Reaction time
Time frame: Baseline and through study completion, an average of 10 weeks.
Memory
Time frame: Baseline and through study completion, an average of 10 weeks.
Attention
Time frame: Baseline and through study completion, an average of 10 weeks.
Working Memory
Time frame: Baseline and through study completion, an average of 10 weeks.
Verbal fluency
Time frame: Baseline and through study completion, an average of 10 weeks.
Questionnaires and Scales
Time frame: Baseline and through study completion, an average of 10 weeks.
Questionnaires and Scales
Time frame: Every week
Questionaires and Scales
Time frame: Every two weeks
Questionnaires and Scales
Time frame: Every three weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Sep 2018.
- Derived from this study: PubMed 42712702Navarro-Lomas G, De-la-O A, Dote-Montero M, Castillo MJ, Amaro-Gahete FJ, Plaza-Florido A. Moderate alcohol intake and heart rate variability adaptations to high-intensity interval training in healthy young adults: the BEER-HIIT study. Front Cardiovasc Med. 2026 Aug 25;13:1920023. doi: 10.3389/fcvm.2026.1920023. eCollection 2026.
- Derived from this study: PubMed 32460793Molina-Hidalgo C, De-la-O A, Dote-Montero M, Amaro-Gahete FJ, Castillo MJ. Influence of daily beer or ethanol consumption on physical fitness in response to a high-intensity interval training program. The BEER-HIIT study. J Int Soc Sports Nutr. 2020 May 27;17(1):29. doi: 10.1186/s12970-020-00356-7.
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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. This study is not recruiting at the moment.
Manuel J. Castillo Garzón principal investigator
Universidad de Granada
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing HIIT-AB Group, HIIT-NAB Group and HIIT-SW Group in people with Drinking, Alcohol and Exercise, run by Universidad de Granada at 1 site in Spain.
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 8 inclusion and 7 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: finished, as of the sponsor's last update on 6 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Physical Fitness Cardiorespiratory fitness (time frame: Baseline and through study completion, an average of 10 weeks.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03660579, which also lists 2 linked publications.
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 6 Sep 2018.