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Deterioration, ClinicalThe ORIENT-RRTNCT07897851

The Orientation Intervention to Rapid Response Teams (ORIENT-RRT) Study: A Quasi-Experimental Study

A study testing Orientation day with rapid response nurse in people with Deterioration, Clinical, run by University of Colorado, Denver at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study will measure knowledge, confidence, and nursing practice outcomes related to the effectiveness and feasibility of a 12-hour educational clinical intervention for NGNs during orientation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Deterioration, Clinical
What is being tested?
Orientation day with rapid response nurse
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
1 siteUnited States
Study dates
28 Sep 2026to 31 Dec 2028
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • New graduate nurses hired onto an acute care unit at University of Colorado Hospital, Medical Center of the Rockies, and Poudre Valley Hospital

Who cannot join

  • New graduate nurses who are not employed on an acute care unit at the three study hospital at UCHealth
  • New graduate nurses who have completed clinical orientation or started orientation prior to this study commencing

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Maureen Varty, PhD, RN contact

720-848-6648

maureen.varty@uchealth.org

United States1 site, 1 recruiting
  • UCHealth

    Aurora, Colorado, 80045

    Maureen Varty, PhD, RN, 7208486648, maureen.varty@uchealth.org

    Karen Hessler, PhD, RN

    Recruiting

Other trials in United States

About this study

This study will measure knowledge, confidence, and nursing practice outcomes related to the effectiveness and feasibility of a 12-hour educational clinical intervention for NGNs during orientation.

Read the detailed description

New graduate nurses (NGN) are faced with multiple challenges as they orient to their role as a registered nurse. Acute care NGN are charged with caring for an increasingly complex patients with high acuity. When a patient begins to decline in the inpatient setting, it is termed patient deterioration. Patient deterioration is defined in differing ways depending on the disposition of the patient and their particular clinical picture, but the term generally refers to a patient who is declining in health rapidly due to acute adverse events during their hospitalization. This study will measure knowledge, confidence, and nursing practice outcomes related to the effectiveness and feasibility of a 12-hour educational clinical intervention for NGNs during orientation.

Being tested
Orientation day with rapid response nurse
Keywords
confidence, knowledge, nursing practice
Medical subject headings
Clinical Deterioration

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Orientation day with rapid response nurseOther

    Also called orientation

    This orientation day is spending attending rapid responses with a rapid response nurse.

Study groups in NCT07897851
Study groupRoleWhat they receive
InterventionExperimentalThis group of newly graduate will spend one day of orientation with a rapid response nurse
Receives: Other: Orientation day with rapid response nurse
ControlNo interventionThis group of new graduate nurses will receive routine orientation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Clinicians' Attitudes towards Responding and Escalating care of Deteriorating patients scale (CARED)

    Assessment of 1) beliefs about rapid response systems, 2) fears about escalating care, and 3) perceived confidence in responding. This is a 22-item scale which uses a 5-point Likert scale. Scores ranges from 22-110. Higher scores indicate that participants have increase confidence that rapid response teams will support them, decreased fears about engaging with rapid response teams, and increase confidence with responding to deteriorating patients.

    Measured: The participants will complete a baseline survey (pre-survey) at enrollment at the start of their orientation. Approximately 10-12 weeks later, the participants will complete a post-survey after they have completed orientation.

  2. Activation of Rapid Responses

    Assessment of whether new graduate nurse or virtual intensive care unit initiated rapid response. New graduate nurse initiation of rapid response demonstrates frontline nurse detected the patient deterioration versus a late recognition by the virtual intensive care unit.

    Measured: Participant's engagement with the rapid response team will be examined from the beginning of their orientation through the end of their first year (52 weeks in total).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Oct 2026
  2. Study start28 Sep 2026
  3. Primary completion30 Sep 2028 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

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
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
Quasi-experimental, two group design
Masking
None (open label)
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07897851
Sponsor's protocol ID
26-1210
Acronym
The ORIENT-RRT
Status last verified
Oct 2026
First submitted
12 Oct 2026
Last updated
27 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Chua WL, Tee A, Hassan NB, Jones D, Tam WWS, Liaw SY. The development and psychometric evaluation of the Clinicians' Attitudes towards Responding and Escalating care of Deteriorating patients scale. Aust Crit Care. 2021 Jul;34(4):340-349. doi: 10.1016/j.aucc.2020.08.008. Epub 2020 Oct 23.

    PubMed 33250402
  • Orique SB, Despins L, Wakefield BJ, Erdelez S, Vogelsmeier A. Perception of clinical deterioration cues among medical-surgical nurses. J Adv Nurs. 2019 Nov;75(11):2627-2637. doi: 10.1111/jan.14038. Epub 2019 Aug 27.

    PubMed 31012138
  • Murray M, Sundin D, Cope V. New graduate nurses' clinical safety knowledge by the numbers. J Nurs Manag. 2019 Oct;27(7):1384-1390. doi: 10.1111/jonm.12819. Epub 2019 Jul 22.

    PubMed 31230379
  • Jones D, Mitchell I, Hillman K, Story D. Defining clinical deterioration. Resuscitation. 2013 Aug;84(8):1029-34. doi: 10.1016/j.resuscitation.2013.01.013. Epub 2013 Jan 31.

    PubMed 23376502
  • Geist NC, Browning M, Messick A. Development of a Critical Reflection Mentorship Program to Enhance Critical Thinking Among Novice Nurses. J Contin Educ Nurs. 2024 Sep;55(9):456-460. doi: 10.3928/00220124-20240718-01. Epub 2024 Aug 1.

    PubMed 39088688

Questions about this trial

What is this clinical trial studying?

A study testing Orientation day with rapid response nurse in people with Deterioration, Clinical, run by University of Colorado, Denver 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: looking for participants now, as of the sponsor's last update on 27 Oct 2026. 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?

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 Maureen Varty, PhD, RN (720-848-6648, maureen.varty@uchealth.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinicians' Attitudes towards Responding and Escalating care of Deteriorating patients scale (CARED) (time frame: The participants will complete a baseline survey (pre-survey) at enrollment at the start of their orientation. Approximately 10-12 weeks later, the participants will complete a post-survey after they have completed orientation.). 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?

On the ClinicalTrials.gov record for NCT07897851, which also lists 5 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 27 Oct 2026.

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