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NCT07631026 · ClinicalTrials.gov registry record · NA

Wearable Device Tracked Recovery From Autologous Breast Reconstructive Surgery

A NA study, sponsored by M.D. Anderson Cancer Center.

Not yet
Registry status
NA
Development phase
50
Enrollment target

NCT07631026: Clinical Trial NA study, sponsored by M.D. Anderson Cancer Center.

NCT07631026 is a NA study that has not yet begun recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 50 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07631026, a NA study, has not yet begun recruiting, sponsored by M.D. Anderson Cancer Center.

NOT YET RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

The purpose of this research study is to learn more about how patients recover after DIEP flap breast reconstruction. We will use a wrist worn activity tracker (Fitbit Inspire 3) to measure steps, heart rate, and sleep before and after surgery, and we will compare this information with short questionnaires about your recovery. The information we learn may help improve patient counseling and design future recovery programs.

Interventions

  • BEHAVIORAL Questionnaires

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2026-12-31
Est. Completion 2029-12-31
Phase NA

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT07631026

The ClinicalTrials.gov registry entry for NCT07631026 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Questionnaires is the first listed.

NCT07631026 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07631026 about?

NCT07631026 is a clinical study titled "Wearable Device Tracked Recovery From Autologous Breast Reconstructive Surgery". The purpose of this research study is to learn more about how patients recover after DIEP flap breast reconstruction. We will use a wrist worn activity tracker (Fitbit Inspire 3) to measure steps, heart rate, and sleep before and after surgery, and we will compare this information with short questio...

What is the current status of trial NCT07631026?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2026-12-31. Estimated completion is 2029-12-31.

What interventions are being tested in trial NCT07631026?

The interventions under investigation include: Questionnaires (BEHAVIORAL).

Who is sponsoring clinical trial NCT07631026?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.