Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06210204 · ClinicalTrials.gov registry record · NA

Improving Access to Surgical Care: Safety, Efficacy, and Satisfaction With Postoperative Telehealth

A NA study, sponsored by VA Eastern Colorado Health Care System.

Not yet
Registry status
NA
Development phase
3,000
Enrollment target

NCT06210204: Clinical Trial NA study, sponsored by VA Eastern Colorado Health Care System.

NCT06210204 is a NA study that has not yet begun recruiting, run by VA Eastern Colorado Health Care System. The registered enrollment target is 3,000 participants, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (114% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06210204, a NA study, has not yet begun recruiting, sponsored by VA Eastern Colorado Health Care System.

NOT YET RECRUITING
Registry status
NA
Development phase
3,000 participants
Enrollment target

Study Summary

Background: A quarter of US Veterans reside in rural communities and are significantly older than their urban counterparts. Providing timely access to care is especially important in this older, independent and medically complex cohort. Virtual care, by phone or video, has improved access to care in non-surgical specialties; however, its utilization in surgery is less than 10% and has continued to decline after the COVID pandemic. Recent studies in surgical patients have demonstrated no difference in missed adverse events, emergency department visits or readmissions; but these data are limited to routine, low-risk procedures in large, urban centers. Routine telehealth for low and high-complexity surgery could be of particular benefit to rural patients by reducing travel challenges, costs, improving scheduling flexibility and reinforcing independence. The hypothesis is that routine telehealth follow-up for elective surgical procedures, of all complexity, will provide equivalent outcomes and improved patient satisfaction and access in comparison to face-to-face follow-up. Significance: VA Integrated Service Network (VISN) 19 is the largest geographic region in the VA system and includes four intermediate/complex VA Medical Centers (VAMC) serving rural and urban patients across 10 states. Almost 4000 unique patients are seen annually at these 4 centers resulting in 2600 operations and over 16,000 patient encounters. Another 2500 unique patients are referred to community care (CC) at a cost of over $5 million in FY23. Improving access through telehealth in this largely rural VISN will positively impact Veterans and reduce community care expenditures in addition to improving patient and provider satisfaction. Innovation \& Impact: There are currently no funded or published randomized trials evaluating the efficacy of telehealth in providing postoperative surgical care to rural patients. The proposal will provide robust, Level 1 data confirming the safety of postoperati

Primary Outcome

Complications that could have been identified with routine follow-up

Interventions

  • OTHER Telehealth follow-up

Trial Details

FieldValue
Enrollment Target 3,000 participants
Start Date 2025-01
Est. Completion 2027-07
Phase NA

What is known before NCT06210204 opens enrollment

NCT06210204 is an interventional study that assigns participants to a tested intervention. Its 3,000 participants enrollment target places it among the larger protocols in the corpus, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (114% higher).

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

NCT06210204 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06210204 about?

NCT06210204 is a clinical study titled "Improving Access to Surgical Care: Safety, Efficacy, and Satisfaction With Postoperative Telehealth". Background: A quarter of US Veterans reside in rural communities and are significantly older than their urban counterparts. Providing timely access to care is especially important in this older, independent and medically complex cohort. Virtual care, by phone or video, has improved access to care in...

What is the current status of trial NCT06210204?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 3,000 participants. The study started on 2025-01. Estimated completion is 2027-07.

What interventions are being tested in trial NCT06210204?

The interventions under investigation include: Telehealth follow-up (OTHER).

Who is sponsoring clinical trial NCT06210204?

This trial is sponsored by VA Eastern Colorado Health Care System, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06210204's enrollment target sits among peer trials

3,000 40th of 2000 higher than 1,959 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00004847 · 3,000 participants · Phase 1

    Diagnosis of Pheochromocytoma

  • NCT00478712 · 3,000 participants

    Hirschsprung Disease Genetic Study

  • NCT00579566 · 3,000 participants

    Novel Biochemical and Molecular Determinants for Soft Tissue Sarcoma

  • NCT00816114 · 3,000 participants

    Chart Review Study of Chronic Myelogenous Leukemia (CML) Patients Treated With Imatinib Outside of a Clinical Trial

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT06210204, the US trial registry maintained by the National Library of Medicine. NCT06210204 (large enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.