Background: Virtual reality (VR) is increasingly used for adjunctive relaxation training in psychiatric care. However, evidence remains limited among hospitalized patients with depressive disorders, particularly in routine inpatient settings in China, and little is known about whether improvement varies by session frequency. Objective: This retrospective study examined whether adjunctive VR-based relaxation training was associated with changes in depressive and anxiety symptoms among inpatients with depressive disorders and whether improvement differed by session frequency. Methods: We conducted a retrospective, nonrandomized natural-group comparison using complete anonymized medical records from patients hospitalized in Lishui Second People’s Hospital between January 1 and December 31, 2022. Patients met () diagnostic criteria for depressive episodes or recurrent depressive disorders and were screened using predefined criteria. The analytic sample included 133 inpatients: 63 (47.4%) received adjunctive VR-based relaxation training plus usual care and 70 (52.6%) received usual care only. Usual care included pharmacotherapy and physiotherapy. The VR intervention consisted of 25-minute immersive relaxation sessions delivered approximately 3 times per week. Symptoms were assessed at admission and discharge using the 17-item Hamilton Depression Scale and Hamilton Anxiety Rating Scale. Response was defined as a reduction of 50% or more from baseline, and remission was defined as a total score of 7 or less. Baseline characteristics, outcome scores, response and remission rates, and exploratory session-frequency subgroups were compared. All analyzed variables were checked against complete medical records; no missing values were identified, and no imputation was performed. Results: The VR and control groups did not differ significantly in baseline depressive or anxiety scores. At discharge, adjunctive VR-based relaxation training was associated with lower depressive and anxiety symptom scores than usual care alone. The VR group also showed higher response rates for both depressive and anxiety symptoms and a higher anxiety remission rate, whereas depression remission was similar. Exploratory session-frequency analyses suggested that anxiety improvement may be more consistently associated with VR exposure than depression remission; however, the pattern was not strictly linear and should be interpreted cautiously because treatment frequency was linked to hospitalization duration and routine care factors. Conclusions: This study is innovative in evaluating structured VR-based relaxation training as an adjunct to routine inpatient depression care and in providing preliminary observations on session-frequency patterns in a real-world Chinese psychiatric setting. Unlike many previous VR studies conducted in noninpatient, nonclinical, or short-term experimental contexts, this study reflects everyday clinical practice among hospitalized patients with depressive disorders. The findings contribute practical evidence for integrating immersive relaxation into comprehensive inpatient care, particularly when additional anxiety relief is desired. Because the study was retrospective and nonrandomized, the findings indicate associations rather than causal effects and should be confirmed in prospective randomized controlled trials.
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Exploring Informal Caregivers’ Perception of the Olera Digital Caregiving Assistance Platform for Dementia Care: Mixed Methods Evaluation Study
Linguistic Fidelity and Classification Performance of Large Language Models for Generating Synthetic Operative Notes: Evaluation Study
Background: Machine learning models for surgical applications require large, diverse datasets; however, data scarcity remains a critical limitation due to privacy regulations, institutional variability, and the rarity of many surgical procedures. Large language models (LLMs) offer a potential solution through synthetic data generation, but their performance and reliability in specialized surgical domains remain underexplored. Objective: This study aimed to evaluate the linguistic fidelity of LLM-generated operative notes for cleft lip and palate procedures and to assess their impact on natural language processing classifier performance under varying data availability conditions. Methods: A total of 630 authentic operative notes were obtained from cleft procedures (86 primary cleft lip repairs, 101 primary cleft palate repairs, and 62 primary alveolar bone grafting [ABG] procedures) performed between 2013 and 2024. GPT-4o generated matched synthetic notes using multishot prompting with anonymized examples. Linguistic fidelity was evaluated using BERTScore for semantic similarity, Jensen-Shannon divergence of part-of-speech trigrams for syntactic structure, and Bilingual Evaluation Understudy (BLEU) scores for lexical overlap. Binary classifiers using ClinicalBERT embeddings and logistic regression were trained under both full data and data-scarce (retaining 5% or 10% of positive training cases while retaining the full negative training set) conditions, with and without synthetic augmentation at approximate ratios of synthetic to real notes (1:1, 2:1, 5:1, and 10:1). Results: Synthetic notes demonstrated high semantic fidelity across all procedures (BERTScore -score: 0.86‐0.88) and low syntactic divergence (Jensen-Shannon divergence: 0.06‐0.08). BLEU scores indicated moderate lexical variation (0.14‐0.19), reflecting distinct but contextually consistent phrasing. With full datasets, synthetic augmentation did not meaningfully affect classifier performance. Under data-scarce conditions retaining 5% of positive training cases while preserving the full negative training set, the area under the curve improved from 0.915 (SD 0.056) to 0.929 (SD 0.033) for cleft lip and from 0.935 (SD 0.036) to 0.949 (SD 0.033) for cleft palate, with smaller gains for ABG (mean 0.983, SD 0.014 to mean 0.987, SD 0.015). When retaining 10% of positive training cases, performance changes were minor across procedures (cleft lip: mean 0.952, SD 0.036 to mean 0.948, SD 0.028; cleft palate: mean 0.945, SD 0.044 to mean 0.956, SD 0.036; and ABG: mean 0.989, SD 0.008 to mean 0.985, SD 0.012). Conclusions: LLM-generated operative notes exhibit strong semantic and syntactic fidelity to authentic documentation and can enhance model performance in a task-dependent manner when authentic data are limited. These findings suggest that synthetic data generation may address data scarcity challenges in specialized surgical domains, particularly for rare or underrepresented procedures, enabling robust machine learning model development.
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Automatic Speech Recognition and Acoustic Analysis for Dysarthria Assessment in Telerehabilitation: User-Centered Design and Usability Study
Background: Dysarthria is a frequent motor speech disorder following a stroke, affecting up to 42% of survivors and resulting in reduced speech intelligibility and diminished quality of life. Clinical assessments, such as the Frenchay Dysarthria Assessment, Second Edition (FDA-2), rely heavily on the subjective judgment of speech-language pathologists (SLPs), which limits comparability and scalability. Telepractice solutions have the potential to extend access to care, but validated digital tools that combine automatic analysis with clinically usable interfaces remain scarce. Objective: This study aimed to develop and evaluate a web-based application that integrates automatic speech recognition (ASR) and acoustic analysis into a user-centered dashboard for SLPs. Specifically, we investigated: (1) whether ASR can provide intelligibility scores comparable to those of human listeners; (2) the usability of the system in 2 iterative cycles with SLPs; and (3) the feasibility of presenting clinically relevant acoustic features to support telerehabilitation. Methods: A user-centered design process was followed, involving contextual inquiry, requirements gathering, prototype development, and iterative testing with SLPs. The analytical core of the prototype included an ASR module (Whisper Large-v3) to compute intelligibility scores, combining word error rate–based accuracy with sentence-level and word-level alignment. Phoneme-level error highlighting was implemented to identify frequent substitution or deletion patterns. In parallel, an acoustic module extracted clinically relevant measures, including fundamental frequency (mean and range), intensity (mean and variability), and vowel formants (F1–F2 space), supplemented by sustained phonation duration. A pilot validation compared ASR-based intelligibility scores with transcriptions from 8 lay listeners for 3 patients with dysarthria performing the Frenchay Dysarthria Assessment–2 word and sentence tasks. Usability was evaluated in 2 cycles with 8 and 4 SLPs, respectively, using the System Usability Scale and structured questionnaires. Results: In the pilot validation, ASR performance was comparable to, and in some cases better than, untrained human listeners for individuals with mild and moderate dysarthria, though performance declined with severe cases. Both usability cycles yielded excellent System Usability Scale scores (cycle 1: mean 88.4, SD 4.6; cycle 2: mean 91.7, SD 4.1). Core workflow elements, including navigation, session upload, and intelligibility score presentation, were consistently rated highly. Feedback evolved from bug reports and requests for clearer terminology in cycle 1 to suggestions for advanced analytic features in cycle 2, such as additional voice-quality indices and integrated note-taking. Conclusions: The prototype demonstrates that automatic intelligibility scoring and acoustic analysis can be integrated into a clinically usable, web-based dashboard. While current limitations include reliance on English-only phoneme analysis, limited advanced acoustic features, and lack of regulatory compliance, the application achieved excellent usability and shows promise for scalable telerehabilitation. Future work should expand multilingual support, incorporate additional acoustic measures, and validate the tool in larger clinical cohorts.
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Digital Cognitive Behavioral Therapy for Older Adults With Symptoms of Depression: Feasibility Cohort Study
A device that revives eyeballs from dead donors could make eye transplants possible
It’s not easy to transplant a whole human eye. The surgery is difficult. And the eyes themselves start to degenerate as soon as they’ve left the body. When surgeons attempted it a few years ago, the newly-transplanted eye wasn’t able to see.
But researchers believe they might have a solution: a device that maintains and revives freshly removed eyeballs using a technique called perfusion. Perfusion works by providing surgically-removed organs with some of the oxygen and nutrients they typically get when they’re inside a body. Treated eyes don’t degrade as quickly, and appear to retain the ability to transmit electrical signals, and potentially see. The device could one day make eye transplantations a viable possibility.
“It’s really cool,” says Shannon Tessier at Massachusetts General Hospital, who was not involved in the research but studies perfusion of other organs. “It could be a new frontier for retina preservation.”
Pia Cosma at the Centre for Genomic Regulation at the Barcelona Institute of Science and Technology in Spain and her colleagues have spent years developing their device. The Eye-in-a-Care-Box (ECaBox), as they call it, delivers an oxygen-rich supply of fluid through the artery that normally supplies the eye with blood.
The eye itself sits on a “bed,” and excess fluids are drained away. And while the device itself is sealed to maintain a specific temperature and pressure, a clear window on its side allows researchers to study and image the eye while it’s inside.
Cosma and her colleagues started experimenting with pig eyes, which are anatomically similar to human eyes but easier to get hold of (the team got theirs from a local slaughterhouse).
Pig eyes that are kept at room temperature outside of the device start to degenerate pretty quickly. The team found that cells in the eye shrank, and the eyes started to lose their structure. Cooling the organs didn’t help preserve them, either—the eyes degenerated within 24 hours even when they were kept at 4°C (39°F).
But eyes kept in the EcABox fared much better. 24 hours later, tests suggested the prefused eyes were “significantly more viable” than eyes that hadn’t been maintained in the device.
The perfused eyes also seemed to be able to respond to light, suggesting they might technically be able to see if they were transplanted. Untreated pig eyes lost this ability as soon as they were removed from the animal. But it came back after about 15 minutes of perfusion, according to the scientists behind the work. A few of the treated eyes kept going for 10 hours or more.
Cosma and her colleagues described the work in a preprint article that has not yet been peer reviewed, and did not want to comment on the work.
After success with the pig eyes, the team members then tested their device on human eyes. They first collected 12 eyes from six people who had died. In each case, one of each pair of eyes was put in the device, while the other was not. Again, the perfused eyes did better—and their retinas were preserved.
Cosma and her colleagues hope that their device could offer scientists a new way to study eye treatments—one that doesn’t involve experimenting on living animals. They also hope that, with some improvements, the ECaBox might provide a way to maintain and revive donated human eyes for whole-eye transplantation.
Whole-eye transplants have been attempted in the past, mostly in research animals, with limited success. In May 2023, a team at NYU Langone transplanted an eye along with part of a face to a man who had survived a high-voltage electrical accident that resulted in the loss of much of the left side of his face, including his left eye, two years earlier. Although the man recovered well, he wasn’t able to see out of the transplanted eye.
We won’t know whether eyes treated in the ECaBox could do any better until they have been transplanted, says Tessier.
In the meantime, Cosma and her colleagues plan to use a newer version of their device to collect more human eyes for research. “We are planning to develop a portable, surgery-room ECaBox to minimize [degradation] in heart-beating donor eyes, when they become available,” they write.

