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LymphomaNCT07390071

Multimodal Telerehabilitation in Patients Undergoing CAR-T Cell Immunotherapy

A study testing Home Automated Telemanagement (HAT) Patient Unit in people with Lymphoma and Myeloma, run by University of Utah at 1 site in United States.

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

The proposed multimodal telerehabilitation model allows a rehabilitation therapy team to set up individualized rehabilitation plans using a web-based care management portal and monitor patient progress online. Read more about this study

Who is it for?
Ages 21 years and older
Conditions the study is for
Lymphoma, Myeloma, Cytokine Release Syndrome
What is being tested?
Home Automated Telemanagement (HAT) Patient Unit
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteUnited States
Study dates
1 Sep 2025to Jan 2029
Phase
Interventional
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 21 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • age >21
  • confirmed diagnosis of lymphoma or myeloma
  • commercial FDA-approved CAR-T delivery planned for ≥4 weeks following enrollment
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
  • Access to a working telephone line in their home or a cell phone.

Who cannot join

  • have unstable angina, uncontrolled hypertension, recent myocardial infarction, pacemakers, painful or unstable bony metastases, or recent skeletal fractures;
  • are engaged in a regular exercise rehabilitation program;
  • have relocation plans within next 6 months;
  • participate in another clinical trial.

Trial locations and contacts

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

United States1 site, 1 recruiting
  • Huntsman Cancer Institute at University of Utah

    Salt Lake City, Utah, 84112

    Douglas Sborov, MD, MS, 801-585-3229, Douglas.Sborov@hci.utah.edu

    Recruiting

Other trials in United States

About this study

The proposed multimodal telerehabilitation model allows a rehabilitation therapy team to set up individualized rehabilitation plans using a web-based care management portal and monitor patient progress online. Patients at home follow a safe and effective personalized exercise and nutrition plan guided by interactive touch-screen technology combined with behavioral counseling, social support, and interactive education and empowerment. The design of the telerehabilitation system is based on the cloud-based Internet-of-Things architecture allowing real-time monitoring of cardiovascular parameters and exercise performance. The patient's level of exertion during exercise is automatically identified by a validated AI-driven algorithm supporting exercise safety and efficacy. The ultimate goal of this pilot feasibility project is to establish the extent of the impact of the proposed patient-centered cancer telerehabilitation model on disease-specific quality of life, and functional and symptom outcomes and to obtain sufficient evidence for a definitive randomized clinical trial evaluating this approach in a multi-center study.

Read the detailed description

CAR-T therapy is a relatively new, innovative treatment strategy to manage refractory hematological cancers, including some types of leukemia, lymphoma, and multiple myeloma (Efficace, 2022). This pivotal treatment has become a standard-of-care for certain malignancies, such as relapsed non-Hodgkins lymphoma, relapsed or refractory acute lymphoblastic leukemia, and relapsed refractory multiple myeloma, with some studies showing at least 80% of the patients with a positive response to treatment (June, 2018; Landry, 2020). While CAR T-cell therapy has led to significant advances in the treatment of hematologic malignancies, it also presents a set of unique toxicities. The two most common acute adverse effects are cytokine release syndrome (CRS) and neurological toxicity known as immune effector cell-associated neurotoxicity syndrome (ICANS), respectively (Neelapu, 2017).

Recent studies suggest that there should be an emphasis on prehabilitation soon after initiating the workup process for CAR-T therapy, maintaining function during active treatment, and close follow-up with rehabilitation especially if neurological sequelae persist (Obaisi, 2022; Kiefer, 2023). Effective interventions are urgently needed to improve the QoL and functional capacity in patients with hematological cancers undergoing CAR-T therapy (Cenik, 2020;Jeevanantham, 2021). Physical activity programs have been shown to impact psychological symptoms, fatigue, and quality of life (Vermaete, 2013, 2014). Crucially, no evidence has been presented to date for patients with hematologic malignancies while undergoing CAR-T therapy. Thus, studies exploring approaches to expand access to multimodal cancer rehabilitation practices in these patients are necessary to address the needs of the rapidly growing population of cancer survivors receiving CAR-T therapy. Recent systematic reviews demonstrated the high potential of telehealth approaches to facilitate cancer rehabilitation (Brick, 2022; Chang, 2022).

Home Automated Telemanagement (HAT). The HAT system is a telemedicine platform supporting patients in following individualized self-care plans and assisting healthcare practitioners in the treatment and monitoring of their patients according to evidence-based guidelines (Finkelstein, 2012; Fleg, 2020; Shero, 2022). HAT is based on the chronic disease care model (Grover, 2014) and provides support for patient self-management, comprehensive patient-provider communication, and multidisciplinary care coordination (Drouin, 2015). The main objective of the HAT system is to minimize the burden of chronic disease management and to simplify monitoring in ambulatory care. To achieve this goal, the HAT system is required (1) to support a constant information feedback loop between the patient and health care providers; (2) to take over all routine repetitive tasks; and (3) to provide real-time clinical decision support both for the patient and clinician. HAT has been successfully implemented and tested in a variety of chronic diseases.

Patient units are used at patient homes to guide patients in following their treatment plans including exercise and diet prescriptions, monitor patients' progress and symptoms, and to communicate with health care providers. Any web-enabled device can serve as a patient unit including touchscreen tablets, VR headsets, and smartphones. The home unit interface underwent rigorous usability testing (Jeong, 2015; Finkelstein, 2021; Gabriel, 2023) and is very simple to operate, even by those without any prior computer experience. The clinician units (any web-enabled device) are used to set up and update individualized treatment plans, analyze patient self-testing results, and review computer-generated alerts. The HAT server implements computerized decision support based on individualized alert setup and realtime monitoring of patient self-testing data. In this study, the HAT system will be focused on the delivery of a multimodal cancer rehabilitation program comprising individualized therapeutic physical exercise, nutrition plan, behavioral counseling, and tailored educational empowerment targeting the social, cognitive, reproductive, and vocational needs of blood cancer survivors.

The proposed multimodal telerehabilitation model allows a rehabilitation therapy team to set up individualized rehabilitation plans using a web-based care management portal and monitor patient progress online. Patients at home follow a safe and effective personalized exercise and nutrition plan guided by interactive touch-screen technology combined with behavioral counseling, social support, and interactive education and empowerment. The design of the telerehabilitation system is based on the cloud-based Internet-of-Things architecture allowing real-time monitoring of cardiovascular parameters and exercise performance. The patient's level of exertion during exercise is automatically identified by a validated AI-driven algorithm supporting exercise safety and efficacy. The ultimate goal of this pilot feasibility project is to establish the extent of the impact of the proposed patient-centered cancer telerehabilitation model on disease-specific quality of life, and functional and symptom outcomes and to obtain sufficient evidence for a definitive randomized clinical trial evaluating this approach in a multi-center study.

This study will determine if patients with hematologic malignancies undergoing CAR-T therapy will demonstrate sufficient acceptability and adherence to the multimodal cancer telerehabilitation, and it will be associated with a positive trajectory of QoL, fitness, and patient-reported outcomes. This trial is an exploratory sequential mixed methods design to assess the feasibility of a patient-centered, culturally tailored telemedicine approach for multimodal cancer rehabilitation in patients with hematologic malignancies undergoing CAR-T therapy.

Eligible patients will undergo a four-week multimodal prehabilitation before the commencement of the CAR-T therapy and then receive continuous online empowerment and education support during CAR-T therapy while undergoing chemotherapy, CAR-T infusion, toxicity monitoring, and recovery for up to four weeks, depending on a specific CAR-T treatment regimen. This will be followed by a twelve-week multimodal telerehabilitation after treatment completion and hospital discharge. A comprehensive assessment will be conducted at the beginning of the study, and the patients will be individually prescribed resistance, aerobic, and relaxation exercises, and a nutrition plan for 4-week prehabilitation based on patient fitness levels and nutrition status. A mobile app will provide interactive education on cancer survivorship, early mobilization, and post-discharge self-care during CAR-T treatment comprising outpatient chemotherapy, CART infusion, and in-patient hospitalization for toxicity monitoring. After the hospital discharge, a 12-week multimodal rehabilitation plan will be provided via the telerehabilitation system which uses validated AI-driven real-time assessment of exercise exertion (Smiley, 2024). Social support will be delivered via group telecounseling sessions. Automated analysis of daily exercise and nutrition logs will alert the telerehabilitation team about low patient adherence and prompt tailored feedback by the telerehabilitation team. The acceptability, usability, feasibility, and adherence will be assessed at the end of the study as described in the Analysis Plan. Finally, this study will assess QoL, fitness, body composition, cancer symptoms, behavioral characteristics, and satisfaction with care before and after the multimodal rehabilitation delivered via a telemedicine platform.

Being tested
Home Automated Telemanagement (HAT) Patient Unit
Medical subject headings
Lymphoma, Neoplasms, Plasma Cell, Cytokine Release Syndrome

What participants receive

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

  • Home Automated Telemanagement (HAT) Patient UnitDevice

    HAT (Home Automated Telemanagement) patient unit will guide patients in following their treatment plans, including exercise and diet prescriptions, monitor patients' progress and symptoms, and communication with health care providers.

    Participants will receive an internet-enabled device, either a touchscreen tablet or a virtual reality (VR) headset, as part of the patient unit, based on their personal preference. Participants will also be provided a pulse oximeter to monitor their heart rate and oxygen saturation, and a fitbit to assess daily physical activity and step counts.

Study groups in NCT07390071
Study groupRoleWhat they receive
Multimodal Cancer TelerehabilitationExperimentalEach enrolled patient will undergo a four-week multimodal prehabilitation before the commencement of the CAR-T therapy. During CAR-T therapy, the patients will use an interactive app supporting cancer self-care education and early mobilization while undergoing chemotherapy, infusion, in-hospital toxicity monitoring, and recovery (the duration depends on the specific CAR-T treatment regimen). After completion of the CAR-T procedures and hospital discharge, the patients will undergo a 12-week home-based multimodal telerehabilitation. Individualized rehabilitation plans using a web-based care management portal. Patients at home follow a safe and effective personalized exercise and nutrition plan guided by interactive touch-screen technology combined with behavioral counseling, social support, and interactive education and empowerment.
Receives: Device: Home Automated Telemanagement (HAT) Patient Unit

What is being measured

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

  1. System Usability Score - Feasibility

    To assess the feasibility of a multimodal cancer telerehabilitation model in patients with hematologic malignancies undergoing CAR-T therapy by evaluating system usability, acceptability, and exercise adherence. This outcome measure will report the System Usability Score for home telerehabilitation in patients undergoing CAR-T therapy.

    The System Usability Scale (SUS) is a 10-item, 5-point Likert questionnaire that yields a single usability score on a 0-100 scale; the minimum possible score is 0 (worst perceived usability) and the maximum is 100 (best perceived usability). This outcome measure will report the mean System Usability Score at 12 weeks after completion of the CAR-T procedure.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  2. Adherence Indicators - Feasibility

    To assess the feasibility of a multimodal cancer telerehabilitation model in patients with hematologic malignancies undergoing CAR-T therapy by evaluating daily exercise logs. This outcome measure will report adherence based on daily exercise logs in patients utilizing the home telerehabilitation after undergoing CAR-T therapy.

    Adherence will be defined as the percentage of exercise sessions of the total number of prescribed exercise sessions.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

Secondary outcomes (13)
  1. 6-minute walk distance (6MWD)

    6MWD is an assessment of functional and aerobic capacity by measuring how far a patient can walk over 6 minutes.

    This outcome measure will report mean 6MWD.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  2. Short Physical Performance Battery (SPPB)

    The Short Physical Performance Battery (SPPB) is a series of assessments to measure balance, strength, and physical functioning. SPPB scores range from 0-12, with lower scores indicating severe limitations and higher scores indicating better physical functioning.

    This outcome measure will report mean SPPB.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  3. Godin Leisure Score Index

    Godin Leisure Score Index is a questionnaire to assess time spent in leisure exercise. Godin Leisure Score Index is a continuous index, with a minimum of 0. Lower scores indicate lower activity and higher cores indicate higher activity.

    This outcome measure will report mean Godin Leisure Score Index.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  4. Extended Activities of Daily Living (ADL)

    The Extended ADL scale is an assessment of functional independence. Extended ADL is a 22-item questionnaire, with each item scaled from 0 to 3.

    The Extended ADL total score ranges from 0 to 66, with lower scores indicating better functional independence and higher scores indicating worse functional independence.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  5. 36-Item Short Form Survey (SF-36)

    SF-36 is a questionnaire that assesses patient health. This outcome measure will report 8 sub-scores: physical function, pain, limitations due to physical health issues, limitations due to personal/emotional issues, emotional well-being, social functioning, energy/fatigue, and general health perceptions.

    Each sub-score ranges from 0-100, with higher score indicating more favorable health and lower score indicating less favorable health.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  6. European Organization For Research And Treatment Of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)

    EORTC QLQ-C30 is a questionnaire to assess health-related quality of life in cancer patients. Patients indicate which symptoms/problems they have experienced during the past week, from "1 Not at All" to "4 Very Much".

    The assessment will report data as 15 subscales with scores from 0-100. A high score indicates a higher response level.

    A high functional scale score (FS) represents a high/healthy level of function and includes Physical, Role, Emotional, Cognitive, and Social functioning. A high symptom scale score (SS) represent a high level of symptomatology/problems and includes Fatigue, Nausea and vomiting, Pain, Dyspnoea, Insomnia, Appetite loss, Constipation, Diarrhoea, Financial difficulties, and Global health status/QoL.

    This outcome will report the mean score of each subscale.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  7. Functional Assessment of Cancer Therapy-Fatigue (FACT-F)

    The FACT-F is a self-reported evaluation of fatigue in cancer patients. This questionnaire has patients rank statements regarding Physical, Social/Family, Emotional, and Functional well-being and Fatigue from 0 "Not at All" to 4 "Very Much".

    The FACT-F has a minimum of 0 and a maximum of 52, with higher scores indicating less fatigue and lower scores indicating more fatigue.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  8. Numeric Rating Scale (NRS)

    NRS is a single-item question assessing pain. NRS scores range from 0-10, with lower scores indicating less pain and higher scores indicating more pain.

    This outcome measure will report mean NRS.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  9. Exercise Self-Efficacy Scale (EXSE)

    The EXSE assesses exercise self-efficacy, or a patient's belief in their ability to continue regular exercise.

    Outcome Expectations for Exercise Scale is an 8-item questionnaire. Each item is a 10-point scale, ranging from 0% (NOT AT ALL CONFIDENT) to 100% (Highly CONFIDENT).

    Total score ranges from 0 to 100, with lower scores indicating worse exercise self-efficacy and higher scores indicating better exercise self-efficacy.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  10. Behavioral Regulation in Exercise Questionnaire 3 (BREQ-3)

    BREQ-3 is an assessment measuring a patient's exercise motivation. BREQ-3 reports 6 sub-scores: Amotivation and External, Introjected, Identified, Integrated, and Intrinsic regulation.

    BREQ-3 score ranges from 0 to 96. Lower scores indicate lower motivation, and higher scores indicate higher motivation.

    This outcome measure will report the mean BREQ-3.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  11. Outcome Expectations for Exercise Scale

    The Outcome Expectations for Exercise Scale assesses beliefs and attitudes about the benefits of exercise.

    Outcome Expectations for Exercise Scale is a 15-item questionnaire. Each item is a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree).

    Total score ranges from 15 to 75, with lower scores indicating worse exercise attitudes and higher scores indicating better exercise attitudes.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  12. Medical Outcome Study (MOS) Exercise Adherence Questionnaire

    The MOS Exercise Adherence Questionnaire assesses patient adherence to exercise.

    MOS Exercise Adherence Questionnaire is a 40-item questionnaire. Scores range from 0 to 100, with lower scores indicating worse exercise adherence and higher scores indicating better exercise adherence.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

  13. Telerehab user attitudes

    Telerehab user attitudes measure patients' overall feelings about remote rehabilitation technology and service. The minimum possible score is 11 (worst perceived attitude) and the maximum is 55 (best perceived attitude).

    This outcome measure will report the mean Telerehab user attitudes at 12 weeks after completion of the CAR-T procedure.

    Measured: up to 12 weeks after completion of the CAR-T procedures.

Timeline

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

  1. First posted5 Feb 2026
  2. Study start1 Sep 2025
  3. Primary completionJan 2029 (estimated)
  4. Study completionJan 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07390071
Sponsor's protocol ID
HCI190212
Status last verified
Jan 2026
First submitted
28 Jan 2026
Last updated
5 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, Filiberti A, Flechtner H, Fleishman SB, de Haes JC, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993 Mar 3;85(5):365-76. doi: 10.1093/jnci/85.5.365.

    PubMed 8433390
  • Acharya UH, Dhawale T, Yun S, Jacobson CA, Chavez JC, Ramos JD, Appelbaum J, Maloney DG. Management of cytokine release syndrome and neurotoxicity in chimeric antigen receptor (CAR) T cell therapy. Expert Rev Hematol. 2019 Mar;12(3):195-205. doi: 10.1080/17474086.2019.1585238. Epub 2019 Mar 18.

    PubMed 30793644
  • Alfano CM, Cheville AL, Mustian K. Developing High-Quality Cancer Rehabilitation Programs: A Timely Need. Am Soc Clin Oncol Educ Book. 2016;35:241-9. doi: 10.1200/EDBK_156164.

    PubMed 27249704
  • AlJohi AA, Aljehani GH, AlSaeed SA, Alhoqail H, Mohammed J, Madi SM. Evidence-based exercises intervention in adults diagnosed with Lymphoma. Saudi Med J. 2022 May;43(5):441-450. doi: 10.15537/smj.2022.43.5.20210894.

    PubMed 35537731
  • Amatya B, Khan F, Lew TE, Dickinson M. Rehabilitation in patients with lymphoma: An overview of Systematic Reviews. J Rehabil Med. 2021 Mar 17;53(3):jrm00163. doi: 10.2340/16501977-2810.

    PubMed 33710351
  • Amireault S, Godin G, Lacombe J, Sabiston CM. The use of the Godin-Shephard Leisure-Time Physical Activity Questionnaire in oncology research: a systematic review. BMC Med Res Methodol. 2015 Aug 12;15:60. doi: 10.1186/s12874-015-0045-7.

    PubMed 26264621
  • Barnett-Page E, Thomas J. Methods for the synthesis of qualitative research: a critical review. BMC Med Res Methodol. 2009 Aug 11;9:59. doi: 10.1186/1471-2288-9-59.

    PubMed 19671152
  • Bedra M, Wick E, Brotman D, Finkelstein J. Avatar-based interactive ileostomy education in hospitalized patients. Stud Health Technol Inform. 2013;190:83-5.

    PubMed 23823383
  • Bedra M, McNabney M, Stiassny D, Nicholas J, Finkelstein J. Defining patient-centered characteristics of a telerehabilitation system for patients with COPD. Stud Health Technol Inform. 2013;190:24-6.

    PubMed 23823363
  • Bedra M, Finkelstein J. Feasibility of post-acute hip fracture telerehabilitation in older adults. Stud Health Technol Inform. 2015;210:469-73.

    PubMed 25991191
  • Benzo R. Satori: Awakening to Outcomes That Matter: The Impact of Social Support in Chronic Obstructive Pulmonary Disease. Ann Am Thorac Soc. 2017 Sep;14(9):1385-1386. doi: 10.1513/AnnalsATS.201707-526ED. No abstract available.

    PubMed 28862500
  • Blanchard CM, Courneya KS, Rodgers WM, Murnaghan DM. Determinants of exercise intention and behavior in survivors of breast and prostate cancer: an application of the theory of planned behavior. Cancer Nurs. 2002 Apr;25(2):88-95. doi: 10.1097/00002820-200204000-00002.

    PubMed 11984095
  • Borrell-Vega J, Esparza Gutierrez AG, Humeidan ML. Multimodal Prehabilitation Programs for Older Surgical Patients. Anesthesiol Clin. 2019 Sep;37(3):437-452. doi: 10.1016/j.anclin.2019.04.004. Epub 2019 Jun 26.

    PubMed 31337477
  • Brennan L, Sheill G, O'Neill L, O'Connor L, Smyth E, Guinan E. Physical Therapists in Oncology Settings: Experiences in Delivering Cancer Rehabilitation Services, Barriers to Care, and Service Development Needs. Phys Ther. 2022 Mar 1;102(3):pzab287. doi: 10.1093/ptj/pzab287.

    PubMed 35084029
  • Brick R, Padgett L, Jones J, Wood KC, Pergolotti M, Marshall TF, Campbell G, Eilers R, Keshavarzi S, Flores AM, Silver JK, Virani A, Livinski AA, Ahmed MF, Kendig T, Khalid B, Barnett J, Borhani A, Bernard G, Lyons KD. The influence of telehealth-based cancer rehabilitation interventions on disability: a systematic review. J Cancer Surviv. 2023 Dec;17(6):1725-1750. doi: 10.1007/s11764-022-01181-4. Epub 2022 Feb 26.

    PubMed 35218521

Questions about this trial

What is this clinical trial studying?

A study testing Home Automated Telemanagement (HAT) Patient Unit in people with Lymphoma and Myeloma, run by University of Utah at 1 site in United States.

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 5 inclusion and 4 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 5 Feb 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 United States. 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 Aileen Gabriel (801-585-3229, aileen.gabriel@utah.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

System Usability Score - Feasibility (time frame: up to 12 weeks after completion of the CAR-T procedures.). The study lists 2 primary outcomes in all. 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 NCT07390071, which also lists 183 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 5 Feb 2026.

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