All Eligible ED Patients (Not Limited to a Particular Condition)JUICEDNCT02506478
Juice Preference in the Emergency Department
An observational study of All Eligible ED Patients (Not Limited to a Particular Condition), run by Hennepin Healthcare Research Institute at 1 site in United States.
Trial summary
ED patients who are able to drink juice will be approached and asked their beverage preference. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- All Eligible ED Patients (Not Limited to a Particular Condition)
- What is being tested?
- Beverage procurement
- How many people
- 385 participants
- Where
- 1 siteUnited States
- Study dates
- May 2015to Sep 2016
- Phase
- Observational
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: All Emergency Department patients, of any age, who are cleared by their treating physician to drink juice, and are able to communicate a juice preference.
Who may be able to join
- All Emergency Department patients, of any age, who are cleared by their treating physician to drink juice, and are able to communicate a juice preference. Patients are only enrolled during randomly selected 1-hour blocks once per week for 26 weeks.
Who cannot join
- Previously enrolled in the study
- Patients who are placed in the "special care" unit of the Emergency Department, which generally cares for intoxicated patients.
Trial locations and contacts
1 site in 1 country.
United States1 site
Hennepin County Medical Center
Minneapolis, Minnesota, 55415
About this study
Official title: Journey to Understand and Interpret Juice Preference in the Emergency Department
ED patients who are able to drink juice will be approached and asked their beverage preference.
Read the detailed description
Once per week for 26 weeks, patients will be enrolled during a randomly selected 1-hour block. The random blocks will be assigned using STATA. During these enrollment periods, all current ED patients will be screened by the treating physicians and research associates, excluding patients in the "Special Care" unit, where most patients are intoxicated with alcohol.
Eligibility for oral consumption of water and juice will be determined by treating physicians. Patients who are deemed eligible to drink water or juice will be approached and asked their beverage preferences. Their response will be recorded, and the beverage will be procured for them.
- Being tested
- Beverage procurement
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Beverage procurementOther
All Emergency Department patients will be approached to ask their beverage preferences in a randomly permuted data collection form. If they would like juice, the flavor will be recorded and the juice (and/or water) will be procured by a research assistant if the patient would like that, though the actual procurement of the juice is not part of the study.
| Study group | Role | What they receive |
|---|---|---|
| ED patients | All ED patients who are able to drink water/juice, and be able to communicate juice preference. Receives: Other: Beverage procurement |
What is being measured
The primary outcome is the main question the study is designed to answer.
Juice preference
Cranberry, apple, orange, or grape
Measured: 1 hour
Secondary outcomes (3)
Beverage preference
Water, juice, or both
Measured: 1 hour
Ice preference
Yes or no (in any beverage)
Measured: 1 hour
Alternate juice preference
For those requesting juice, they will be asked if there is an unavailable alternate flavor that he/she would prefer
Measured: 1 hour
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jul 2015 (estimated)
- Study startMay 2015
- Primary completionSep 2016
- Study completionSep 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for All Eligible ED Patients (Not Limited to a Particular Condition)Studies 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
- Observational
- Time perspective
- Cross-sectional
- Enrolment
- 385 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hennepin Healthcare Research Institute
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Brian Driver, Hennepin Healthcare Research Institute
- Investigators
- Brian E Driver, MD, Principal investigator, Hennepin Healthcare Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02506478
- Sponsor's protocol ID
- 15-3980
- Acronym
- JUICED
- Status last verified
- Dec 2016
- First submitted
- 15 Jun 2015
- Last updated
- 28 Dec 2016
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Dec 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Journey to Understand and Interpret Juice Preference in the Emergency Department
- ClinicalTrials.gov ID
- NCT02506478
- Acronym / sponsor ID
- JUICED / 15-3980
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 385 participants (actual)
- Lead sponsor
- Hennepin Healthcare Research InstituteUniversity, hospital or other
- Study start
- May 2015
- Primary completion
- Sep 2016 (actual)
- Study completion
- Sep 2016 (actual)
- First posted
- 23 Jul 2015 (estimated)
- 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.
ED patients who are able to drink juice will be approached and asked their beverage preference.
Detailed description
Once per week for 26 weeks, patients will be enrolled during a randomly selected 1-hour block. The random blocks will be assigned using STATA. During these enrollment periods, all current ED patients will be screened by the treating physicians and research associates, excluding patients in the "Special Care" unit, where most patients are intoxicated with alcohol.
Eligibility for oral consumption of water and juice will be determined by treating physicians. Patients who are deemed eligible to drink water or juice will be approached and asked their beverage preferences. Their response will be recorded, and the beverage will be procured for them.
Study design
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| ED patients | – | Other: Beverage procurementAll ED patients who are able to drink water/juice, and be able to communicate juice preference. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All Emergency Department patients, of any age, who are cleared by their treating physician to drink juice, and are able to communicate a juice preference.
Key inclusion criteria (1 listed)
- All Emergency Department patients, of any age, who are cleared by their treating physician to drink juice, and are able to communicate a juice preference. Patients are only enrolled during randomly selected 1-hour blocks once per week for 26 weeks.
Key exclusion criteria (2 listed)
- Previously enrolled in the study
- Patients who are placed in the "special care" unit of the Emergency Department, which generally cares for intoxicated patients.
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 |
|---|---|---|
| Beverage procurementAll Emergency Department patients will be approached to ask their beverage preferences in a randomly permuted data collection form. If they would like juice, the flavor will be recorded and the juice (and/or water) will be procured by a research assistant if the patient would like that, though the actual procurement of the juice is not part of the study. | Other | ED patients |
Primary outcome
Juice preference
Time frame: 1 hour
Cranberry, apple, orange, or grape
3 secondary outcomes
Beverage preference
Time frame: 1 hour
Ice preference
Time frame: 1 hour
Alternate juice preference
Time frame: 1 hour
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 28 Dec 2016.
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.
Brian E Driver, MD principal investigator
Hennepin Healthcare Research Institute
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of All Eligible ED Patients (Not Limited to a Particular Condition), run by Hennepin Healthcare Research Institute at 1 site in United States.
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 1 inclusion and 2 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 28 Dec 2016. 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 United States. 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?
Juice preference (time frame: 1 hour). 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 28 Dec 2016; AzTrials last refreshed its copy on 1 Nov 2026.