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RECRUITING NA

Function After Anterior Cervical Discectomy and Fusion Surgery: Timing of Physical Therapy

NCT06202443 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this two-group randomized clinical trial is to examine the effects of early postoperative PT compared to delayed postoperative PT for improving outcomes after hospital discharge for ACDF surgery. The main question this clinical trial aims to answer are: * Whether early PT participants will demonstrate greater improvements in outcomes compared to delayed PT participants. * Whether improvements in handgrip strength, cervical endurance, and cervical range of motion will be associated with improvements in outcomes. Participants will be randomized to one of two groups (early PT or delayed PT) and outcomes compared across groups.

Interventions

  • OTHER Early PT
  • OTHER Delayed PT

Study Locations (4)

Hawaii

  • Tripler Army Medical Center — Honolulu

Tennessee

  • Vanderbilt University Medical Center — Nashville

Texas

  • Booke Army Medical Center — Fort Sam Houston

Washington

  • Madigan Army Medical Center — Tacoma

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2024-02-01
Est. Completion 2027-07-31
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06202443

The ClinicalTrials.gov registry entry for NCT06202443 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 695 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Cervical Spine Degeneration appearing as the primary indexed condition, and to 2 interventions — of which Early PT is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06202443 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Hawaii, Tennessee, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06202443 about?

NCT06202443 is a clinical study titled "Function After Anterior Cervical Discectomy and Fusion Surgery: Timing of Physical Therapy". The goal of this two-group randomized clinical trial is to examine the effects of early postoperative PT compared to delayed postoperative PT for improving outcomes after hospital discharge for ACDF surgery. The main question this clinical trial aims to answer are: * Whether early PT participants ...

What is the current status of trial NCT06202443?

This trial is currently recruiting. It is a NA study. The enrollment target is 76 participants. The study started on 2024-02-01. Estimated completion is 2027-07-31.

What conditions does trial NCT06202443 study?

This clinical trial studies the following conditions: Cervical Spine Degeneration, ACDF Surgery. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06202443?

The interventions under investigation include: Early PT (OTHER), Delayed PT (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06202443?

This trial is sponsored by Vanderbilt University Medical Center, which has 695 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06202443 being conducted?

This trial has 4 study locations across Hawaii, Tennessee, Texas, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial