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Clinical Decision Support System (CDSS)CDSS-ADOPTNCT07398235

A Qualitative Study Examining Clinical Decision Support System Adoption Among Hospital Clinicians

An observational study of Clinical Decision Support System (CDSS), run by Medway NHS Foundation Trust at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A Qualitative Study to Explore the Barriers to Adoption of Clinical Decision Support Systems Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Clinical Decision Support System (CDSS)
What is being tested?
Semi-structured interview
How many people
18 participants
Where
1 siteUnited Kingdom
Study dates
10 Jan 2026to 16 Mar 2026
How long will I take part?
1 Day
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
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Hospital clinicians employed by Medway NHS Foundation Trust

Who may be able to join

  • Employed by Medway NHS Foundation Trust at the time of recruitment
  • Working clinically within the Emergency Department
  • Clinical grade of FY1, FY2, SHO/CTF, SAS/Registrar, Consultant, Nurse, Advanced Clinical practitioner, Physician Assistant, or Clinical Support Worker
  • Involved in the assessment and management of adult emergency department patients
  • Have routine access to the Trust electronic patient record system (Sunrise EPR) during clinical duties
  • Able to provide informed consent to participate
  • Aged 18 years or older

Who cannot join

  • Bank, agency, or locum staff who are not permanently or regularly employed by the department.
  • Staff currently on leave, secondment, or not actively practising in the ED during the data collection period.
  • Clinicians currently involved in the design, management, or evaluation of the CDSS system under study.

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Medway NHS Foundation Trust

    Gillingham, Kent, ME7 5NY

Other trials in United Kingdom

About this study

Official title: A Qualitative Study to Explore the Barriers to Adoption of Clinical Decision Support Systems

A Qualitative Study to Explore the Barriers to Adoption of Clinical Decision Support Systems

Read the detailed description

Qualitative study looking at clinical decision support system adoption among clinicians in a district general hospital. This will involve semi-structured interviews of various clinical staff in the emergency department, looking at work-habits regarding clinical decision support tool use.

Being tested
Semi-structured interview

What participants receive

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

  • Semi-structured interviewOther

    A 20-30 minute semi-structured interview using the pre-defined topic sheet

Study groups in NCT07398235
Study groupRoleWhat they receive
FY1/2Foundation Year 1 \& 2 Doctors
Receives: Other: Semi-structured interview
SHOSenior House Officer level doctor above FY2 but below Registrar
Receives: Other: Semi-structured interview
RegistrarRegistrar level doctor
Receives: Other: Semi-structured interview
ConsultantConsultant level doctor
Receives: Other: Semi-structured interview
Physician AssistantPhysician Assistant clinician
Receives: Other: Semi-structured interview
ACPAdvanced Clinical Practitioner
Receives: Other: Semi-structured interview
CSWClinical Support Worker
Receives: Other: Semi-structured interview
NurseRegistered Nurse
Receives: Other: Semi-structured interview

What is being measured

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

  1. Saturation of Themes Related to Barriers to CDSS Adoption

    The primary outcome examines the barriers to clinical decision support system adoption, such as hardware issues, governance concerns, user-interface problems, and trusted information. These themes will be examined during interviews with open-ended questions to allow user experiences to be recorded.

    This study will use purposive sampling with maximum variation to ensure representation across key categories of Emergency Department clinicians who use clinical decision support systems (CDSS). Participants will be selected to capture a range of roles and experiences, including Advanced Clinical Practitioners (ACPs), Physician Associates (PAs), Clinical Support Workers (CSWs), nurses, and doctors at different levels (Foundation Year 1-2, Senior House Officers, Registrars, and Consultants). Recruitment will continue until data saturation of themes related to CDSS adoption is achieved within and across these categories, anticipated at approximately one to two participants per role group.

    Measured: The study ran between 10th January 2026 until 31 January 2026. The study was considered complete once all planned participant interviews have been conducted or recruitment has formally ceased following achievement of data saturation.

Timeline

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

  1. First posted9 Feb 2026
  2. Study start10 Jan 2026
  3. Primary completion31 Jan 2026
  4. Study completion16 Mar 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
18 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07398235
Sponsor's protocol ID
1366
Other IDs
IRAS ID: 365984
Acronym
CDSS-ADOPT
Status last verified
May 2026
First submitted
19 Jan 2026
Last updated
18 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Mebrahtu TF, Skyrme S, Randell R, Keenan AM, Bloor K, Yang H, Andre D, Ledward A, King H, Thompson C. Effects of computerised clinical decision support systems (CDSS) on nursing and allied health professional performance and patient outcomes: a systematic review of experimental and observational studies. BMJ Open. 2021 Dec 15;11(12):e053886. doi: 10.1136/bmjopen-2021-053886.

    PubMed 34911719
  • Meunier PY, Raynaud C, Guimaraes E, Gueyffier F, Letrilliart L. Barriers and Facilitators to the Use of Clinical Decision Support Systems in Primary Care: A Mixed-Methods Systematic Review. Ann Fam Med. 2023 Jan-Feb;21(1):57-69. doi: 10.1370/afm.2908.

    PubMed 36690490
  • Chen W, O'Bryan CM, Gorham G, Howard K, Balasubramanya B, Coffey P, Abeyaratne A, Cass A. Barriers and enablers to implementing and using clinical decision support systems for chronic diseases: a qualitative systematic review and meta-aggregation. Implement Sci Commun. 2022 Jul 28;3(1):81. doi: 10.1186/s43058-022-00326-x.

    PubMed 35902894
  • Liberati EG, Ruggiero F, Galuppo L, Gorli M, Gonzalez-Lorenzo M, Maraldi M, Ruggieri P, Polo Friz H, Scaratti G, Kwag KH, Vespignani R, Moja L. What hinders the uptake of computerized decision support systems in hospitals? A qualitative study and framework for implementation. Implement Sci. 2017 Sep 15;12(1):113. doi: 10.1186/s13012-017-0644-2.

    PubMed 28915822
  • Sutton RT, Pincock D, Baumgart DC, Sadowski DC, Fedorak RN, Kroeker KI. An overview of clinical decision support systems: benefits, risks, and strategies for success. NPJ Digit Med. 2020 Feb 6;3:17. doi: 10.1038/s41746-020-0221-y. eCollection 2020.

    PubMed 32047862

Questions about this trial

What is this clinical trial studying?

An observational study of Clinical Decision Support System (CDSS), run by Medway NHS Foundation Trust at 1 site in United Kingdom.

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 7 inclusion and 3 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 18 May 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 Kingdom. 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?

Saturation of Themes Related to Barriers to CDSS Adoption (time frame: The study ran between 10th January 2026 until 31 January 2026. The study was considered complete once all planned participant interviews have been conducted or recruitment has formally ceased following achievement of data saturation.). 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 NCT07398235, 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 18 May 2026.

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