Patients' Perceptions and Comprehension of Original Versus AI-Generated Plain Language Summaries of Cochrane Oncology Systematic Reviews
| Registry | NCT07140107 |
| Status | Enrolling by invitation |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: triple, supportive care |
| Enrollment | 130 (Estimated) |
| Sponsor | University of Split, School of Medicine (Other); collaborators: University Hospital of Split |
| Conditions | Non-Metastatic Breast Cancer |
| Interventions | AI-generated PLS, Original PLS (Behavioral) |
| Dates | start 2025-08-14, primary completion 2026-02-01 (estimated), completion 2026-02-01 (estimated), first posted 2025-08-24, last updated 2025-08-24 |
| Locations | 1 site in Croatia |
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-Summary
The study explores how patients with non-metastatic breast cancer perceive and comprehend original Plain Language Summary and AI-generated Plain Language Summary (PLS) of two systematic reviews from the Cochrane Library. The systematic reviews address exercise during adjuvant therapy and psychological interventions for non-metastatic breast cancer. The study, which is randomized and double-blind, aims to assess whether AI-generated PLS and original PLS differ in their influence on patients' intention to undertake and apply the recommendation presented in the summary, as well as their overall understanding of the study results.
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+Detailed description
Studies show that Plain Language Summaries (PLS), which are intended to improve accessibility to health information for laypeople, are lacking in terms of comprehension, readability, and user engagement. Further empirical research is needed to evaluate the comparative effectiveness of AI-generated summaries versus original Plain Language Summaries. This study, conducted at the Department of Oncology and Radiotherapy at the University Hospital of Split aims to explore whether large language models (LLMs), such as ChatGPT, can be leveraged to provide summaries of complex medical content, as those found in systematic reviews, to be more streamlined and adapted for laypeople. The prospective, randomized, single-center, parallel group, double-blind, controlled trial focuses specifically on patients diagnosed with non-metastatic breast cancer, histologically confirmed, and aims to help them make more evidence-based medical decisions regarding their health and recovery. The study's primary objective is to analyze patients' level of intention for changing their behavior and start applying the interventions described in the summary. The level of intention to change behavior will be measured using a visual analog scale ranging from 0 to 100 (0 - do not agree at all and 100 - fully agree). The secondary outcomes are patients' level of understanding calculated by the score received on a five-question knowledge survey (5 as a maximum score), the level of trust in (range 0-100) and clarity of (range 0-100) the information presented in the PLS, and their confidence in their decision to change behavior (range 0-100). The survey is based on the information presented in the PLS and the questions focus on patients' understanding of the benefits and risks of the intervention as well as the quality of evidence described in the systematic reviews. Recruitment for this study will take place over 6 months. Patients will be invited to participate in the study before or after their routine oncology appointment. The participants will read two summaries from two respective Cochrane reviews: exercise during adjuvant therapy and psychological interventions for non-metastatic breast cancer. They will then take the brief survey that tests the impact and likelihood of applying the recommendations described in the summary and their overall understanding of the medical information discussed in the reviews. The study includes female adult oncology patients diagnosed with non-metastatic breast cancer, histologically confirmed, following a modality of the treatment, which includes one or more of the following: neoadjuvant chemotherapy (with or without immunotherapy or antiHER2 therapy); adjuvant chemotherapy (with or without immunotherapy or antiHER2 therapy); adjuvant radiotherapy (including local and locoregional radiation treatment, with possible radiotherapy boost where indicated). Since participants in this study are limited to reading material and completing a survey, the study is non-invasive in nature and poses low-risk. Data will be analyzed using descriptive statistics to summarize participant characteristics and assess baseline comparability between the two study arms.
+Arms and interventions
| Arm | Type | Interventions | Description |
|---|
| Patients Receiving AI-generated Plain Language Summaries | Experimental | Behavioral: AI-generated PLS | Experimental Group: participants in this group receive two AI-generated Plain Language Summaries based on the scientific abstract of two Cochrane systematic reviews: Exercise during Adjuvant Therapy (1) and Psychological Interventions for Non-metastatic Breast Cancer (2). |
| Patients Receiving Original Plain Language Summaries | Active comparator | Behavioral: Original PLS | Active Comparative Group: participants in this group receive two original Plain Language Summaries based on the scientific abstract of two Cochrane systematic reviews: Exercise during Adjuvant Therapy (1) and Psychological Interventions for Non-metastatic Breast Cancer (2). |
- AI-generated PLS (Behavioral): Reading AI-generated Plain Language Summaries of two Cochrane systematic reviews covering the same two evidence-based topics: exercise during adjuvant therapy and psychological interventions for non-metastatic breast cancer.
- Original PLS (Behavioral): Reading original Plain Language Summaries of two Cochrane systematic reviews covering the same two evidence-based topics: exercise during adjuvant therapy and psychological interventions for non-metastatic breast cancer.
+Outcome measures
Primary outcomes
- Patients' level of intention for changing their behavior [Immediately after reading individual PLS]: Patients' level of intention for changing their behavior and start applying the interventions described in the summary, measured on a visual analogue scale (VAS) ranging from 0 to 100 (do not agree at all to 100 fully agree).
Secondary outcomes
- Patients' comprehension of the information presented in the summary [Immediately after reading individual PLS]: Patients' level of understanding of the information presented in the summaries calculated by the score received on a five-question knowledge survey (score range 0-5).
- Patients' level of trust in the information presented [Immediately after reading individual PLS]: Patients' level of trust in the information presented in the summaries, measured on a VAS (range 0-100).
- Patients' level of perceived clarity in the information [Immediately after reading individual PLS]: Patients' level of perceived clarity of the information presented in the summaries, measured on a VAS (range 0-100).
- Patient's level of confidence in their decision to change behavior [Immediately after reading individual PLS]: Patients' level of confidence in the decision to change behavior, measured on a VAS (range 0-100)
+Eligibility
Sex: Female, ages: 18 Years to any
Inclusion Criteria:
* female patients with histologically confirmed non-metastatic breast cancer currently undergoing chemotherapy or radiotherapy:
1. neoadjuvant chemotherapy (with or without immunotherapy or antiHER2 therapy),
2. adjuvant chemotherapy (with or without immunotherapy or antiHER2 therapy),
3. adjuvant radiotherapy (including local and locoregional radiation treatment with possible radiotherapy boost where indicated).
* patients need to be able to read and understand Croatian.
Exclusion Criteria:
* female patients with metastatic breast cancer.
* female patients receiving only hormonal treatment.
+Locations (1)
| Facility | City | Country | Status |
|---|
| Department of Oncology and Radiotherapy, University Hospital Split | Split | Croatia | |
+Publications
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