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Not yet recruitingNCT07552363Updated Apr 27, 2026

ChatGPT-Driven Blended Teaching for Pain Management in Nursing Students: A Randomized Controlled Trial

An interventional study of ChatGPT-Driven Blended Teaching Model for Pain Management and Traditional Clinical Nursing Rounds in Pain Management, Nursing Education and Knowledge, Attitudes, Practice, sponsored by Shahid Beheshti University of Medical Sciences. Not yet recruiting at 1 site in Iran. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-27.

Sponsored by Shahid Beheshti University of Medical Sciences · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
156
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Pain management is a core competency in nursing practice, yet nursing students consistently demonstrate insufficient knowledge, unfavorable attitudes, limited competence, and low self-efficacy in this area. Artificial intelligence (AI)-based educational tools, particularly ChatGPT, have emerged as promising resources in nursing education; however, rigorous experimental evidence on their effectiveness remains scarce.

This study is a two-arm, parallel-group randomized controlled trial (RCT) that aims to evaluate the effect of a ChatGPT-driven blended teaching model for pain management on nursing students' knowledge and attitudes toward pain, nursing competence, and learning self-efficacy.

Eligible nursing students at Shahid Beheshti University of Medical Sciences (Tehran, Iran) will be randomly assigned in a 1:1 ratio to either:

  • Intervention group: ChatGPT-assisted blended clinical nursing rounds (8 sessions over 4 weeks, each 90 minutes, combining bedside rounds with AI-assisted pre- and post-round activities)
  • Control group: Traditional clinical nursing rounds (same number and duration of sessions, without any AI tools)

Outcomes will be measured at baseline (1 week before intervention), immediate post-test (1 week after intervention), and 3-month follow-up using validated instruments: the Nurses' Knowledge and Attitudes Survey Regarding Pain (NKASRP), the Nursing Student Competence Scale (NSCS), and the Nursing Students' Learning Self-Efficacy instrument (NLSE).

Findings will provide empirical evidence to guide educational policy and curriculum design in nursing programs, with the goal of improving pain management education and patient care outcomes.

02

Conditions studied

  • Pain Management
  • Nursing Education
  • Knowledge, Attitudes, Practice

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Keywords

  • ChatGPT
  • Artificial Intelligence
  • Blended Learning
  • Pain Management
  • Nursing Students
  • Clinical Competence
  • Randomized Controlled Trial
03

In context

Behavior

1,573 studies on the registry are indexed under Behavior; 313 are open to participants now.

This study's planned enrollment of 156 is above the median of 120 across 1,197 interventional studies indexed under Behavior.

Browse Behavior studies →

Lead sponsor

Shahid Beheshti University of Medical Sciences is the lead sponsor of 229 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Undergraduate nursing students in their fourth semester or higher, or master's or doctoral nursing students engaged in clinical training involving direct patient care
  2. Provision of electronic
  3. Access to the internet and a personal device (computer, tablet, or smartphone) for the asynchronous components of the blended teaching model
  4. No participation in a formal comprehensive pain management course within the previous 12 months

Exclusion criteria

Exclusion Criteria:

  1. Inability to attend at least one face-to-face session or to complete online activities (e.g., due to repeated absences)
  2. Any self-reported or university-documented cognitive or mental health condition that prevented completion of questionnaires or participation in training
  3. Voluntary withdrawal at any stage of the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
156 participants (estimated)

Study arms

  • Experimental
    ChatGPT-Driven Blended Teaching Group

    Participants receive a blended teaching intervention integrating ChatGPT-assisted instruction with traditional in-person clinical nursing rounds focused on pain management. The intervention consists of 8 sessions over 4 weeks (2 sessions per week), each approximately 90 minutes, comprising three phases: pre-round preparation (30 min) using standardized ChatGPT prompts and case-based learning; bedside nursing round (30 min) with patient assessment and instructor feedback; and post-round activities (30 min) using ChatGPT to resolve uncertainties and complete case reports. Students are organized in groups of 4-6 and rotate through medical, surgical, and chronic pain clinical departments.

    Behavioral: ChatGPT-Driven Blended Teaching Model for Pain Management

  • Active comparator
    Traditional Clinical Nursing Rounds Group

    Participants receive traditional clinical nursing rounds without any ChatGPT or AI components. The instructor selects and introduces clinical cases; students review resources and prepare reports. During rounds, the instructor directs all activities, including case presentation, assessment, nursing diagnosis, intervention, and outcome evaluation. The control group receives an identical number and duration of sessions (8 sessions over 4 weeks, each approximately 90 minutes) in the same clinical departments to ensure exposure consistency.

    Behavioral: Traditional Clinical Nursing Rounds

Interventions

  • BehavioralChatGPT-Driven Blended Teaching Model for Pain Management

    A blended teaching model integrating ChatGPT with in-person clinical nursing rounds for pain management education. Delivered over 4 weeks (8 sessions × 90 minutes). Each session includes: (1) pre-round preparation using standardized ChatGPT prompts for case analysis and evidence retrieval; (2) bedside nursing rounds with pain assessment, patient education, and instructor feedback; and (3) post-round activities using ChatGPT to resolve clinical uncertainties and complete case reports. All ChatGPT outputs were reviewed by supervising faculty for accuracy. Students used pre-designed, standardized prompts based on the WHO analgesic ladder and national clinical protocols.

    Also known as: AI-Assisted Blended Clinical Nursing Rounds

  • BehavioralTraditional Clinical Nursing Rounds

    Standard clinical nursing rounds without AI tools. The instructor directs all activities including case introduction, bedside assessment, nursing diagnosis, intervention planning, and outcome evaluation. Students primarily observe and respond to instructor questions. Sessions match the intervention group in number, duration, and clinical setting (8 sessions × 90 minutes over 4 weeks).

06

What researchers measure

Primary outcomes

  1. Knowledge and Attitudes Toward Pain

    Measured using the Nurses' Knowledge and Attitudes Survey Regarding Pain (NKASRP), a 39-item instrument comprising 22 true/false questions, 13 multiple-choice questions, and 2 case studies. Each correct answer scores 1 point (range: 0-39); results expressed as percentage of correct responses. Higher scores indicate better knowledge and attitudes toward pain management. A Persian forward-backward translation was performed, with face and content validity confirmed by a nursing faculty panel.

    Time frame: Baseline (1 week before intervention), immediate post-test (1 week after intervention), and 3-month follow-up

Secondary outcomes

  1. Nursing Competence

    Measured using the Persian version of the Nursing Student Competence Scale (NSCS), a 28-item instrument across 6 subscales: medical-related knowledge, basic nursing skills, communication and cooperation, lifelong learning, global perspective, and critical thinking. Items rated on a 5-point Likert scale (range: 28-140). Higher scores indicate greater competence. The Persian version demonstrated Cronbach's α = 0.90 and ICC = 0.88.

    Time frame: Baseline (1 week before intervention), immediate post-test (1 week after intervention), and 3-month follow-up

  2. Learning Self-Efficacy

    Measured using the Persian version of the Nursing Students' Learning Self-Efficacy instrument (NLSE), a 21-item instrument across 5 dimensions: conceptual understanding, higher-order cognitive skills, practical work, everyday application, and nursing communication. Items rated on a 5-point Likert scale (range: 21-105). Higher scores indicate greater self-efficacy. The Persian version demonstrated Cronbach's α = 0.93 and ICC = 0.89.

    Time frame: Baseline (1 week before intervention), immediate post-test (1 week after intervention), and 3-month follow-up

07

Study locations

1 site
  • Faculty of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences
    Tehran, Tehran Province, Iran
08

References and documents

Individual participant data

Plan to share: Undecided — Due to privacy considerations, a final decision has not been made at this time.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07552363
Responsible party
Sogand Sarmadi (Shahid Beheshti University of Medical Sciences, Shahid Beheshti University of Medical Sciences) — Principal investigator
First posted
Apr 27, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Dec 1, 2026 (estimated)
Completion
Jan 1, 2027 (estimated)
Last update
Apr 27, 2026

Study contacts

Sogand Sarmadi
Contact
sogand.sarmadi@ymail.com
+989198599908

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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