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Low Back PainNCT07733752

Pre-Visit AI Symptom-Checking and Shared Decision-Making in Spine Physical Therapy

An observational study of Low Back Pain and Neck Pain, run by Assiut University at 1 site in Egypt.

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

Artificial intelligence (AI) symptom-checking tools, including large language models such as ChatGPT, are increasingly used by patients before they seek care. These tools may shape patients' beliefs about their diagnosis, how serious they think their condition is, and when they decide to seek treatment. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Low Back Pain, Neck Pain, Radiculopathy
What is being tested?
re-visit AI symptom-checker use
How many people
200 participants
Where
1 siteEgypt
Study dates
10 Jun 2026to 10 Feb 2027
How long will I take part?
6 Weeks
Phase
Observational
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

Study population: Adults aged 18 years or older presenting for a new evaluation at outpatient physical therapy clinics for a spine-related musculoskeletal complaint - neck, thoracic, or low back pain, with or without radicular symptoms. Consecutive eligible patients are enrolled and grouped by their use of AI-based symptom-checking tools for the current complaint in the 30 days preceding the visit (AI users vs. non-AI users). Patients with recent spinal surgery, serious spinal pathology under active management, cognitive impairment limiting participation, or concurrent enrollment in a study affecting spine-related decision-making are not included.

Who may be able to join

  • Age: 18 years or older
  • Presenting for a new evaluation at an outpatient physical therapy clinic for a spine-related musculoskeletal complaint, including Neck, Thoracic, and Low back pain With or without radicular symptoms
  • Able to provide informed consent.
  • Able to read, understand, and complete study questionnaires

Who cannot join

  • Recent spinal surgery within the past 3 months, due to differing clinical pathways and management strategies.
  • Presence of serious spinal pathology under active medical management, such as:
  • Malignancy (e.g., metastatic disease) Spinal infection Acute fracture
  • Cognitive impairment or other conditions that limit the ability to provide informed consent or reliably complete study measures.
  • Patients currently enrolled in another study that may influence clinical decision-making or outcomes related to spine care.

Trial locations and contacts

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

Mariam A Ibrahim Principal investigator contact

+20 10 01539399

Mariam.A.ibrahim@med.aun.edu.eg

Egypt1 site, 1 recruiting
  • Faculty of Medicine, Assiut University, Egypt

    Asyut

    Mariam A Ibrahim Principal investigator, +20 10 01539399, Mariam.A.ibrahim@med.aun.edu.eg

    Recruiting

Other trials in Egypt

About this study

Official title: When AI Is the First Clinician: Impact of Pre-Visit AI Use on Presentation, Diagnostic Expectations, and Shared Decision-Making in Spine Physical Therapy

Artificial intelligence (AI) symptom-checking tools, including large language models such as ChatGPT, are increasingly used by patients before they seek care. These tools may shape patients' beliefs about their diagnosis, how serious they think their condition is, and when they decide to seek treatment. It is not yet known how this pre-visit AI use affects the initial physical therapy encounter for spine-related problems.

This prospective observational cohort study examines whether prior use of AI symptom-checking tools influences the first physical therapy evaluation in adults presenting with spine-related musculoskeletal complaints (neck, thoracic, or low back pain, with or without radicular symptoms). Consecutive patients attending an outpatient physical therapy clinic for a new evaluation are grouped as AI users or non-AI users based on whether they used such a tool for their current complaint in the previous 30 days.

The primary outcome is shared decision-making, measured with the SDM-Q-9 immediately after the initial evaluation. Secondary outcomes include stage of presentation, agreement between the patient's expected diagnosis and the clinician's classification, baseline pain and disability, functional performance, and clinical outcomes at 2 and 6 weeks. The investigators hypothesize that prior AI use is associated with differences in shared decision-making and in how patients present for care.

Read the detailed description

Background and Rationale AI-based symptom-checking tools, including large language models, are increasingly used by patients as a first point of clinical interpretation before seeking care. Available evidence suggests these tools show moderate and variable diagnostic accuracy and can influence patients' diagnostic beliefs, perceived symptom severity, and healthcare-seeking behavior, raising concerns about pre-diagnostic anchoring. In spine and musculoskeletal care, early presentation, accurate classification, and patient engagement are important determinants of outcomes, and current practice relies on history, physical examination, and shared decision-making under the assumption that patients present without strongly preformed diagnostic expectations. The growing use of AI may alter this dynamic. Evidence on the real-world impact of pre-visit AI use on the physical therapy encounter is currently limited.

Objective The primary objective is to determine whether prior use of AI symptom-checking tools influences shared decision-making during the initial physical therapy evaluation in patients presenting with spine-related musculoskeletal conditions. Secondary objectives examine associations between prior AI use and stage of presentation, agreement between patient-expected and clinician diagnosis, baseline clinical status, functional performance, health-seeking behavior, and short-term clinical outcomes.

Design and Setting This is a prospective observational cohort study conducted in outpatient physical therapy clinics. No study-specific interventions are introduced; all participants receive standard physical therapy care determined by their treating clinician.

Participants and Grouping Consecutive adults (≥18 years) presenting for a new evaluation for a spine-related musculoskeletal complaint (neck, thoracic, or low back pain, with or without radicular symptoms) who can provide informed consent and complete study questionnaires in English are eligible. Patients are excluded for recent spinal surgery within the past 3 months, serious spinal pathology under active medical management (e.g., malignancy, spinal infection, acute fracture), cognitive impairment limiting consent or reliable completion of measures, or current enrollment in another study that may influence clinical decision-making or spine-related outcomes. Participants are classified into two groups based on whether they used an AI symptom-checking tool for their current complaint within the prior 30 days: AI users and non-AI users.

Study Instruments and Measures AI exposure is captured at baseline via a questionnaire assessing AI use (yes/no), tool type, frequency, degree of personalization, and reported influence on care-seeking. Clinical measures include symptom duration, pain intensity (Numeric Pain Rating Scale, 0-10), region-specific disability (Oswestry Disability Index for low back pain or Neck Disability Index for neck pain), and the Five Times Sit-to-Stand test. Diagnostic expectation is assessed by comparing the patient-expected diagnosis with the clinician's classification, categorized as match, partial match, or mismatch. Shared decision-making is measured with the SDM-Q-9 (score range 0-45; higher scores indicate greater patient involvement) immediately after the initial evaluation. Follow-up outcomes at 2 and 6 weeks include pain, disability (ODI/NDI), Global Rating of Change, self-reported adherence, and healthcare utilization.

Procedures At baseline (pre-visit), AI exposure, symptom duration, pain, and disability are collected. During the initial evaluation, the clinician performs a standard physical therapy assessment and classification, and patient expectations are recorded. Immediately post-visit, participants complete the SDM-Q-9. At 2-week and 6-week follow-up, clinical outcomes and adherence are assessed and AI use is re-evaluated. Data are recorded on standardized forms and stored securely using coded identifiers.

Sample Size The primary outcome is SDM-Q-9 following the initial evaluation. Using G*Power (v3.1.9.7), a sample of 128 participants (64 per group) provides 80% power to detect a moderate between-group difference (Cohen's d = 0.5) at a two-sided alpha of 0.05. To account for potential group imbalance and an anticipated attrition of 15-20%, approximately 200 consecutive patients will be recruited.

Statistical Analysis Continuous variables are summarized as mean ± standard deviation and categorical variables as frequencies and percentages. AI users and non-AI users are compared using independent-samples t-tests for continuous variables and chi-square tests for categorical variables. Statistical significance is set at p ≤ 0.05.

Being tested
re-visit AI symptom-checker use
Keywords
Artificial intelligence, ChatGPT, Shared decision-making, SDM-Q-9, Spine, Patient expectations
Medical subject headings
Low Back Pain, Neck Pain, Radiculopathy

What participants receive

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

  • re-visit AI symptom-checker useOther

    Self-reported use of an AI-based symptom-checking tool (e.g., a large language model such as ChatGPT) for the current spine-related complaint during the 30 days before the initial physical therapy evaluation. This exposure occurs naturally prior to presentation and is not assigned by the investigator. Exposure status is ascertained at baseline via a questionnaire capturing whether AI was used (yes/no), the type of tool, frequency of use, degree of personalization, and the reported influence of AI use on care-seeking timing.

Study groups in NCT07733752
Study groupRoleWhat they receive
AI UsersPatients who reported using an AI-based symptom-checking tool (e.g., a large language model such as ChatGPT) for their current spine-related complaint within the 30 days before their initial physical therapy evaluation.
Receives: Other: re-visit AI symptom-checker use
Non-AI UsersPatients who reported no use of any AI-based symptom-checking tool for their current spine-related complaint within the 30 days before their initial physical therapy evaluation.

What is being measured

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

  1. Shared Decision-Making (SDM-Q-9)

    Patient-perceived involvement in shared decision-making during the initial physical therapy evaluation, measured with the 9-item Shared Decision-Making Questionnaire (SDM-Q-9). Raw total score ranges from 0 to 45; higher scores indicate greater perceived patient involvement in decision-making.

    Measured: Immediately after the initial physical therapy evaluation (Day 0)

Secondary outcomes (6)
  1. Stage of Presentation (Symptom Duration)

    Self-reported duration of the current spine-related symptoms, in days, recorded at the initial evaluation as an indicator of timeliness/stage of presentation.

    Measured: At initial evaluation (Day 0)

  2. Diagnostic Agreement (Patient-Clinician Concordance)

    Concordance between the patient's expected diagnosis and the clinician's classification, categorized as 0 = match, 1 = partial match, 2 = mismatch.

    Measured: At initial evaluation (Day 0)

  3. Pain Intensity (Numeric Pain Rating Scale)

    Self-reported pain intensity on the 11-point Numeric Pain Rating Scale (0 = no pain, 10 = worst imaginable pain); higher scores indicate greater pain.

    Measured: Day 0, 2 weeks, 6 weeks

  4. Disability (ODI or NDI)

    Region-specific self-reported disability, using the Oswestry Disability Index for low back pain or the Neck Disability Index for neck pain. Both are scored 0-100% (0 = no disability; higher scores indicate greater disability).

    Measured: Day 0, 2 weeks, 6 weeks

  5. Health-Seeking Behavior (AI Influence on Care Timing)

    Self-reported influence of prior AI symptom-checker use on the timing of seeking care, categorized as earlier, delayed, or no change.

    Measured: At initial evaluation (Day 0)

  6. Adherence and Healthcare Utilization

    Self-reported adherence to the recommended treatment plan.

    Measured: 2 weeks, 6 weeks

Timeline

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

  1. First posted29 Jul 2026
  2. Study start10 Jun 2026
  3. Primary completion10 Dec 2026 (estimated)
  4. Study completion10 Feb 2027 (estimated)

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
200 participants (estimated)
Target duration
6 Weeks
IDs, dates and publications
ClinicalTrials.gov ID
NCT07733752
Sponsor's protocol ID
04-2026-300876
Status last verified
Jun 2026
First submitted
24 Jul 2026
Last updated
29 Jul 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Harvey D, White S, Reid D, Cook C. Patient perspectives of process variables in musculoskeletal care pathways. Musculoskelet Sci Pract. 2025 Apr;76:103287. doi: 10.1016/j.msksp.2025.103287. Epub 2025 Feb 14.

    PubMed 39978029
  • Meyer AND, Giardina TD, Spitzmueller C, Shahid U, Scott TMT, Singh H. Patient Perspectives on the Usefulness of an Artificial Intelligence-Assisted Symptom Checker: Cross-Sectional Survey Study. J Med Internet Res. 2020 Jan 30;22(1):e14679. doi: 10.2196/14679.

    PubMed 32012052
  • Kuroiwa T, Sarcon A, Ibara T, Yamada E, Yamamoto A, Tsukamoto K, Fujita K. The Potential of ChatGPT as a Self-Diagnostic Tool in Common Orthopedic Diseases: Exploratory Study. J Med Internet Res. 2023 Sep 15;25:e47621. doi: 10.2196/47621.

    PubMed 37713254
  • Kumar R, Dougherty C, Sporn K, Khanna A, Ravi P, Prabhakar P, Zaman N. Intelligence Architectures and Machine Learning Applications in Contemporary Spine Care. Bioengineering (Basel). 2025 Sep 9;12(9):967. doi: 10.3390/bioengineering12090967.

    PubMed 41007212
  • Bensel VA, Habeck A, Brunot MH, Becton EJ, Ray M, Brackett AL, Lisi AJ. Artificial intelligence in spine care: A scoping review of treatment applications. N Am Spine Soc J. 2025 Nov 20;25:100827. doi: 10.1016/j.xnsj.2025.100827. eCollection 2026 Mar.

    PubMed 41536317
  • Muelbauer EJ, Alvi MA, Kennedy DJ, Fehlings MG. The future is now: How AI is reshaping spine care. N Am Spine Soc J. 2025 Nov 14;24:100825. doi: 10.1016/j.xnsj.2025.100825. eCollection 2025 Dec.

    PubMed 41458002
  • Rossettini G, Bargeri S, Cook C, Guida S, Palese A, Rodeghiero L, Pillastrini P, Turolla A, Castellini G, Gianola S. Accuracy of ChatGPT-3.5, ChatGPT-4o, Copilot, Gemini, Claude, and Perplexity in advising on lumbosacral radicular pain against clinical practice guidelines: cross-sectional study. Front Digit Health. 2025 Jun 27;7:1574287. doi: 10.3389/fdgth.2025.1574287. eCollection 2025.

    PubMed 40657647
  • Basharat A, Shah R, Wilcox N, Tur G, Tripati S, Kansal P, Gandhi N, Pokuri S, Chong G, Odonkor CA, Varhabhatla N, Chow R. ChatGPT and low back pain - Evaluating AI-driven patient education in the context of interventional pain medicine. Interv Pain Med. 2025 Sep 2;4(3):100636. doi: 10.1016/j.inpm.2025.100636. eCollection 2025 Sep.

    PubMed 40978326
  • Li YH, Li N, Liu ZX, Du S, Shuai Y, Yang R, Xu L, Li X, Jiang Y, Li W. The effectiveness of artificial intelligence health education accurately linking system on self-management in non-specific lower back pain patients. Front Public Health. 2025 Sep 11;13:1630329. doi: 10.3389/fpubh.2025.1630329. eCollection 2025.

    PubMed 41018793
  • Baldus SG, Wiesmann M, Habel U, Gerhards A, Hasan D, Weyland CS, Truhn D, Hasl MM, Clemens B, Nikoubashman O. Patients' views on the use of artificial intelligence in healthcare: Artificial Intelligence Survey Aachen (AISA)-a prospective survey. Insights Imaging. 2026 Jan 5;17(1):6. doi: 10.1186/s13244-025-02159-3.

    PubMed 41491377
  • Alzubaidi H, Hussein A, Mc Namara K, Scholl I. Psychometric properties of the Arabic version of the 9-item Shared Decision-Making Questionnaire: the entire process from translation to validation. BMJ Open. 2019 Apr 4;9(4):e026672. doi: 10.1136/bmjopen-2018-026672.

    PubMed 30948608
  • Algarni AS, Ghorbel S, Jones JG, Guermazi M. Validation of an Arabic version of the Oswestry index in Saudi Arabia. Ann Phys Rehabil Med. 2014 Dec;57(9-10):653-63. doi: 10.1016/j.rehab.2014.06.006. Epub 2014 Aug 4.

    PubMed 25262247
  • Zhou M, Pan Y, Zhang Y, Song X, Zhou Y. Evaluating AI-generated patient education materials for spinal surgeries: Comparative analysis of readability and DISCERN quality across ChatGPT and deepseek models. Int J Med Inform. 2025 Jun;198:105871. doi: 10.1016/j.ijmedinf.2025.105871. Epub 2025 Mar 13.

    PubMed 40107040

Questions about this trial

What is this clinical trial studying?

An observational study of Low Back Pain and Neck Pain, run by Assiut University at 1 site in Egypt.

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 4 inclusion and 5 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 29 Jul 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 Egypt. 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 Mariam A Ibrahim Principal investigator (+20 10 01539399, Mariam.A.ibrahim@med.aun.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Shared Decision-Making (SDM-Q-9) (time frame: Immediately after the initial physical therapy evaluation (Day 0)). 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 NCT07733752, which also lists 13 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 29 Jul 2026.

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