Evidence map›Paper›PMID 37815850›Full record

ArticleJMIR research protocols2023

Digital Phenotyping for Monitoring and Disease Trajectory Prediction of Patients With Cancer: Protocol for a Prospective Observational Cohort Study.

Gabrielė Jenciūtė, Gabrielė Kasputytė, Inesa Bunevičienė, Erika Korobeinikova, Domas Vaitiekus, Arturas Inčiūra, Laimonas Jaruševičius, Romas Bunevičius, Ričardas Krikštolaitis, Tomas Krilavičius and 2 more

Open access · goldAbstract read
In one paragraph

Article in JMIR research protocols, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Observational
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Gabrielė JenciūtėFaculty of Informatics, Vytautas Magnus University, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-7960-5405
Gabrielė KasputytėFaculty of Informatics, Vytautas Magnus University, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-5621-0061
Inesa BunevičienėFaculty of Political Science and Diplomacy, Vytautas Magnus University, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-8330-0399
Erika KorobeinikovaOncology Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-9753-8637
Domas VaitiekusOncology Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-9583-4475
Arturas InčiūraOncology Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.ORCID https://orcid.org/0009-0002-2448-6300
Laimonas JaruševičiusOncology Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-2181-691X
Romas BunevičiusProIT, Vilnius, Lithuania.ORCID https://orcid.org/0009-0004-9541-1554
Ričardas KrikštolaitisFaculty of Informatics, Vytautas Magnus University, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-9556-4121
Tomas KrilavičiusFaculty of Informatics, Vytautas Magnus University, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-8509-420X
Elona JuozaitytėOncology Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-6695-7786
Adomas BunevičiusDepartment of Neurology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, United States.ORCID https://orcid.org/0000-0003-0446-6898
Lithuanian University of Health Sciences · LTVytautas Magnus University · LTColumbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTimely recognition of cancer progression and treatment complications is important for treatment guidance. Digital phenotyping is a promising method for precise and remote monitoring of patients in their natural environments by using passively generated data from sensors of personal wearable devices. Further studies are needed to better understand the potential clinical benefits of digital phenotyping approaches to optimize care of patients with cancer.

objectiveWe aim to evaluate whether passively generated data from smartphone sensors are feasible for remote monitoring of patients with cancer to predict their disease trajectories and patient-centered health outcomes.

methodsWe will recruit 200 patients undergoing treatment for cancer. Patients will be followed up for 6 months. Passively generated data by sensors of personal smartphone devices (eg, accelerometer, gyroscope, GPS) will be continuously collected using the developed LAIMA smartphone app during follow-up. We will evaluate (1) mobility data by using an accelerometer (mean time of active period, mean time of exertional physical activity, distance covered per day, duration of inactive period), GPS (places of interest visited daily, hospital visits), and gyroscope sensors and (2) sociability indices (frequency of duration of phone calls, frequency and length of text messages, and internet browsing time). Every 2 weeks, patients will be asked to complete questionnaires pertaining to quality of life (European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire [EORTC QLQ-C30]), depression symptoms (Patient Health Questionnaire-9 [PHQ-9]), and anxiety symptoms (General Anxiety Disorder-7 [GAD-7]) that will be deployed via the LAIMA app. Clinic visits will take place at 1-3 months and 3-6 months of the study. Patients will be evaluated for disease progression, cancer and treatment complications, and functional status (Eastern Cooperative Oncology Group) by the study oncologist and will complete the questionnaire for evaluating quality of life (EORTC QLQ-C30), depression symptoms (PHQ-9), and anxiety symptoms (GAD-7). We will examine the associations among digital, clinical, and patient-reported health outcomes to develop prediction models with clinically meaningful outcomes.

resultsAs of July 2023, we have reached the planned recruitment target, and patients are undergoing follow-up. Data collection is expected to be completed by September 2023. The final results should be available within 6 months after study completion.

conclusionsThis study will provide in-depth insight into temporally and spatially precise trajectories of patients with cancer that will provide a novel digital health approach and will inform the design of future interventional clinical trials in oncology. Our findings will allow a better understanding of the potential clinical value of passively generated smartphone sensor data (digital phenotyping) for continuous and real-time monitoring of patients with cancer for treatment side effects, cancer complications, functional status, and patient-reported outcomes as well as prediction of disease progression or trajectories. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/49096.

Indexed as

biomarkerbiomarkerscancerdata collectiondata generationdigital phenotypedigital phenotypingmobile phonemodelmodelsmonitormonitoringoncologypredictprediction

Identifiers

PMID37815850
PMCPMC10599285
OpenAlexW4385432289

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.