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Evaluating the Effectiveness of an AI-powered Physician Assistant in Improving Patients' and Physician's Satisfaction in an Outpatient Setting of a Tertiary Care Hospital.

2026年8月7日 更新者:Saqib Bakhshi、Aga Khan University

Patients' satisfaction depends on several factors, including health care costs, access to care, and the waiting time to see a healthcare professional. In Pakistan, hospitals face overcrowding, which in turn results in long waiting times, particularly in outpatient departments. Longer waiting times not only hurt patients' experience and hospitals' performance but also increase stress on the physicians.

These challenges can be addressed with the effective use of Artificial Intelligence (AI) and related technologies. By leveraging machine learning algorithms and advanced data prediction models, AI can augment healthcare providers in clinical decision-making and streamline their work processes. However, these applications are largely studied and implemented in high-income countries, creating a lack of evidence from low- and middle-income countries.

Hence, a randomized controlled trial will be conducted to assess the effectiveness of an AI physician assistant in improving patient and physician satisfaction within outpateint clincis of a resource constrained setting.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

367

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Karachi、パキスタン
        • Aga Khan University Hospital
        • コンタクト:
        • コンタクト:
        • 主任研究者:
          • Saqib Bakhshi

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria (Patients):

  • Informed consent before enrolment.
  • Adults aged 18 years and above.
  • Initial patients registering at the clinic during the entire trial duration.
  • Possession of a digital device for an OTP (one-time password)
  • Can read and write Urdu and/or English

Inclusion Criteria (Physicians):

  • Informed Consent
  • Agree to include AI physician assistant in their workflows

Exclusion Criteria (Patients):

  • Patients requiring emergency care
  • Patients who refuse to complete the history process with the AI physician assistant.

Exclusion Criteria (Physicians):

- Physicians from non-surgical specialties

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:AI Physician Assistant

The intervention group will comprise participants enrolled in the application (AI physician assistant) in addition to the standard of care

The study participant allocated to the intervention will interact with the AI-physician assistant application "Hami" before they consult with the physician. The application will collect the medical history of the patient. This will then be followed by an AI-generated clinical summary, which their physicians will receive before the consultation begins. Physicians will review this summary and ask further questions of patients if required, and update the patient's record through an inbuilt scribe feature in the application.

The intervention evaluated here is an AI Physician Assistant. The assistant takes the patient's history using a specialty-specific line of questioning. Once the interaction ends, the application converts the information into an AI-generated clinical summary for physicians to review.

The physician reviews the summary and asks the patient additional questions, if required. Any additions or changes to the patient's history are recorded in the application. The physician then conducts a physical examination and can view AI-generated and guideline-based recommendations for assessment and treatment within the application. These recommendations may be selected, modified, or disregarded according to the physician's clinical expertise.

All additions to the patient's record can be entered manually or dictated verbally and automatically added through the application's ambient scribe feature. Once the treatment plan has been documented, the application generates a SOAP note.

介入なし:Standard of Care
The arm will comprise participants who receive standard care. In surgical clinics, standard care involves residents seeing the patients before the physicians. However, as part of the study, we will include physicians who agree to see patients without residents taking the history first. Hence, the trial uses the term 'physician' as part of the control group or standard care terminology.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Patient's satisfaction
時間枠:Every day from each patient for a period of 2 months
Patient satisfaction is conceptualized through the lens of perceived quality of care, which is influenced by the effective utilization of waiting time and the provision of patient-centred care. Effective utilization of waiting time refers to patients' perceptions regarding whether their waiting time was used meaningfully during the visit. The domains of patient-centred care have been adapted from the Institute of Medicine (IOM) framework and include respect for patients' values and preferences, coordinated and integrated care, adequacy of information and communication, emotional support, involvement of family and friends, and physical comfort. These questions have been adapted based on the study objectives. The questionnaire will include demographic questions and five-point Likert-scale items (Strongly Agree to Strongly Disagree) and one open-ended question to obtain additional feedback regarding patients' experiences and satisfaction.
Every day from each patient for a period of 2 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Physician Satisfaction
時間枠:From each physician at the end of each day for two months.

It will be assessed with regards to integration of an AI-powered physician assistant, focusing on usability, impact on workflow efficiency, evidence based treatment recommendations and improved patient-physician interaction.

Physician's satisfaction will be calculated utilizing mean scoring system, where each question will be scored on a 5 point Likert scale (Strongly Agree to Strongly Disagree). Additionally, we will ask one open-ended question at the end of the survey as part of physician satisfaction. This tool will be made exclusively for this study and will undergo content validation.

From each physician at the end of each day for two months.
Mean consultation time
時間枠:Every day for each patient consultation for a period of 2 months

Consultation time (calculated in minutes) refers to the time taken by the physician while the patient is in the physician's room and the time taken by the physician for each of the following: to inquire about symptoms, conduct an examination, prescribe treatment, and provide counselling.

It will be measured using timestamps from a stopwatch from the time the patient enters the consultation room till the time they leave.

Every day for each patient consultation for a period of 2 months

その他の成果指標

結果測定
メジャーの説明
時間枠
Process flow evaluation outcome - Mean queuing time
時間枠:Every day for each patient visit for a period of 2 months

Mean queuing time for each patient before the consultation process begins. Queuing time (calculated in minutes) refers to the time spent by a patient in the waiting area after their registration has been completed till the start of their consultation.

It will be recorded using timestamps in two steps: one starting from the registration till the vitals are taken, secondly after vitals have been recorded till the patient visit the physician. These timings will be combined into a single aggregated time and will be calculated once for each patient.

Every day for each patient visit for a period of 2 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2026年11月1日

研究の完了 (推定)

2026年11月1日

試験登録日

最初に提出

2026年8月7日

QC基準を満たした最初の提出物

2026年8月7日

最初の投稿 (実際)

2026年8月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月10日

QC基準を満たした最後の更新が送信されました

2026年8月7日

最終確認日

2026年1月1日

詳しくは

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個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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