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NCT05499663 · ClinicalTrials.gov registry record · Phase 1

Title: Leveraging Technology to Address Health Outcomes of Cancer Survivors

A Phase 1 study of Cancer and Survivorship, sponsored by University of Maryland, Baltimore.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target
1
Study location

NCT05499663: Completed Phase 1 study of Cancer and Survivorship, sponsored by University of Maryland, Baltimore.

NCT05499663 is a Phase 1 study of Cancer and Survivorship that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 51 participants, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05499663, a Phase 1 study of Cancer and Survivorship, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target
1
Study location

Study Summary

At the end of cancer treatment, many patients are still dealing with symptoms of cancer and side effects of treatment. Many are also left in a surreal mental state with uncertainty regarding the future of their health. Survivorship Care Plans are plans that are provided to individuals at the completion of cancer treatment (i.e., chemotherapy, surgery, radiation). Survivorship Care Plans describe the details of a person's diagnosis and treatment, as well as provide recommendations for follow-up appointments, referrals, and healthy behaviors to accelerate recovery and prevent recurrence (e.g., diet, exercise, smoking cessation). Survivorship Care Plans are currently static documents that are provided via paper and become outdated as soon as the person's health status changes. Therefore, there is a need to digitize Survivorship Care Plans to improve the accessibility, modifiability, and longevity of the plan. In addition, with current technology, there is an opportunity for Survivorship Care Plans to be linked with mobile devices and activity trackers so that people can track health behaviors and compare them to their clinical goals, enabling people to take charge of their own health. Charles River Analytics developed an app called POSTHOC (POST-treatment Healthcare Outcomes for Cancer survivors) that digitizes the Survivorship Care Plan with goals to integrate it into the digital medical record. Herein, phase I/II feasibility/preliminary efficacy randomized controlled trial is being conducted among 54 patients with cancer who recently completed adjuvant treatment for cancer (e.g., chemotherapy, radiotherapy, surgery) to compare 12 weeks of the POSTHOC app as part of the Survivorship Care Plan vs. the usual care Survivorship Care Plan on total symptom burden. Participants will be randomized 2:1, POSTHOC:usual care. All participants will be asked to download the POSTHOC app to assess technical compatibility and for data collection purposes (i.e., step count via Fitbit,

Primary Outcome

Number of participants who logged data at least three times in the POSTHOC app

Interventions

  • BEHAVIORAL POSTHOC app

Study Locations (1)

Maryland

  • University of Maryland, Baltimore - Baltimore

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2024-03-05
Est. Completion 2025-03-20
Phase Phase 1
University of Maryland, Baltimore

560 total trials

What the finished NCT05499663 record still lists

NCT05499663 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower).

The record links to 3 conditions, with Cancer appearing as the primary indexed condition, and to 1 intervention - of which POSTHOC app is the first listed.

NCT05499663 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT05499663 about?

NCT05499663 is a clinical study titled "Title: Leveraging Technology to Address Health Outcomes of Cancer Survivors". At the end of cancer treatment, many patients are still dealing with symptoms of cancer and side effects of treatment. Many are also left in a surreal mental state with uncertainty regarding the future of their health. Survivorship Care Plans are plans that are provided to individuals at the complet...

What is the current status of trial NCT05499663?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2024-03-05. Estimated completion is 2025-03-20.

What conditions does trial NCT05499663 study?

This clinical trial studies the following conditions: Cancer, Survivorship, Symptoms and Signs.

What interventions are being tested in trial NCT05499663?

The interventions under investigation include: POSTHOC app (BEHAVIORAL).

Who is sponsoring clinical trial NCT05499663?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05499663 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05499663's enrollment target sits among peer trials

51 420th of 615 higher than 195 of 615 other Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05499663, the US trial registry maintained by the National Library of Medicine. NCT05499663 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.