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

NCT04586296 · ClinicalTrials.gov registry record · NA

Tele-monitoring of Post Join Arthroplasty Outcomes: A Feasibility Study

A NA study, sponsored by University of Alabama at Birmingham.

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT04586296: Completed NA study, sponsored by University of Alabama at Birmingham.

NCT04586296 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04586296, a NA study, has completed, sponsored by University of Alabama at Birmingham.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to develop an effective telephone mediated follow-up system to reduce the number of unplanned readmissions and emergency department visits after total joint arthroplasty. This will help reduce costs related to unnecessary visits to the hospital as well as catch complications earlier on. The investigators plan to accomplish this by performing a pilot study that will compare the outcomes of using an Interactive Voice Response system through phone call in addition to the standard follow-up protocol. The outcomes of this group will be compared to those receiving the standard of care follow-up protocol.

Primary Outcome

VAS is a patient measured scale to evaluate pain, on a scale of 1-10 with 10 being the worst pain.

Interventions

  • OTHER Telemedicine

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2021-03-16
Est. Completion 2023-08-16
Phase NA
University of Alabama at Birmingham

1,160 total trials

What the finished NCT04586296 record still lists

NCT04586296 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT04586296 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04586296 about?

NCT04586296 is a clinical study titled "Tele-monitoring of Post Join Arthroplasty Outcomes: A Feasibility Study". The purpose of this study is to develop an effective telephone mediated follow-up system to reduce the number of unplanned readmissions and emergency department visits after total joint arthroplasty. This will help reduce costs related to unnecessary visits to the hospital as well as catch complicat...

What is the current status of trial NCT04586296?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2021-03-16. Estimated completion is 2023-08-16.

What interventions are being tested in trial NCT04586296?

The interventions under investigation include: Telemedicine (OTHER).

Who is sponsoring clinical trial NCT04586296?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04586296's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 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

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04586296, the US trial registry maintained by the National Library of Medicine. NCT04586296 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.