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NCT05390827From ClinicalTrials.govRecruiting

Remote Digital Physiologic Data Collection in Cancer: An MSK Registry Protocol

Remote Digital Physiological Data Collection in Cancer: An MSK Registry Protocol

  • Solid Tumor

At a glance

Phase
Phase not stated
Study type
Observational
Sponsor
Memorial Sloan Kettering Cancer Center
Enrolment target
3,692
Started
19 May 2022
Main results due
July 2027
Study sites
1
Registry updated
29 September 2026

Can you take part?

  • Aged 18 years and over.
  • Open to any sex.
  • Healthy volunteers can take part.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
Inclusion Criteria:

Project 1: HealthKit

* Individuals who meet at least one of the following criteria:

  * Diagnosis of new onset early-stage (I-III), low-grade (I-II), or locally advanced solid tumor
  * Historical diagnosis of primary invasive solid tumor
  * Diagnosis of metastatic (stage IV) or high-grade (III-IV) disease
  * Enrolled onto an investigational trial in the EDD Service
  * Seen in the MSK UCC from 2021 and onwards
  * Completion of Survivorship Patient Self-Assessment
  * Adult without a history of cancer \<50 years of age
  * Adult without a history of cancer ≥ 50 years of age
* ≥18 years old
* Own an Apple iPhone or Android with valid operating software
* Self-reported "very well" comprehension of written and verbal English language
* Willing and able to provide informed consent and HIPAA authorization for the release of personal health information

Project 2: DigIT-Ex

Individuals who meet one of the following criteria:

* Patients at MSK who are:
* Scheduled to undergo any type of BMT (Cohort 1)
* Diagnosed with new onset AML and scheduled to initiate antineoplastic therapy (Cohort 2)
* Scheduled to undergo any surgery for prostate cancer (Cohort 3)
* Scheduled to undergo any lung cancer surgery (Cohort 4)
* Scheduled to undergo TNT for locally advanced rectal cancer (Cohort 5)
* Scheduled to initiate androgen deprivation therapy for at least 12 months and has one of the following prostate cancer diagnoses (Cohort 6):
* High risk/very high localized, locally advanced,
* Biochemically recurrent prostate cancer
* Treatment naïve, low-volume metastatic prostate cancer
* Scheduled Scheduled to undergo chemotherapy for metastatic pancreatic cancer (Cohort 7)
* Receiving outpatient care at Memorial Sloan Kettering Cancer Center (MSK)(Cohort 10)
* Diagnosed with metastatic cancer to bone For purposes of this study, metastatic bone disease includes skeletal involvement from multiple myeloma (Cohort 10)
* Scheduled for non-emergent orthopaedic surgery to stabilize lower-extremity bone metastases (Cohort 10)
* Able to undergo at least 5 consecutive days of preoperative monitoring prior to surgery (Cohort 10)
* Have had a CT scan including the L3 vertebral level within 3 months before surgery (used to assess skeletal muscle mass and sarcopenia) (Cohort 10)
* Have a ≥50% predicted likelihood of 3-month postoperative survival, as estimated by the PATHFx clinical decision-support tool (Cohort 10
* Individuals without cancer \<50 years of age (Cohort 8)
* Individuals without cancer ≥50 years of age (Cohort 9)

  * 18 to 90 years old at the time of consent
  * Willing and able to download the Withings Health Mate app onto their personal mobile device
  * Willing to provide mobile digital physiological data for a period of at least six months to a maximum of one year following consent for Cohorts 1-9, and 4 months following consent for Cohort 10.
  * Willing to provide informed consent

Exclusion Criteria:

Project 1: HealthKit

* Unable or unwilling to successfully export and /or share physiological data

Project 2: DigIT-Ex

* Unable or unwilling to appropriately use digital platforms or devices
* Require a wheelchair for ambulation (Cohort 10)
* Are undergoing stabilization surgery for a primary bone tumor (rather than metastatic disease) (Cohort 10)

What this study is about

In the sponsor’s own words, from the registry.

The purpose of this study is to develop a secure method of collecting physiologic information from patients with cancer. The researchers will use this information to learn more about how physiologic data may relate to cancer diagnosis and response to treatment, and to identify factors that may lead to higher or lower risk of cancer.

Study sites(1)

  • Memorial Sloan Kettering Cancer Center

    New York, New York, United States

    Recruiting

Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT05390827. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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Remote Digital Physiologic Data Collection in Cancer: An MSK Registry Protocol | Trialion