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NCT06153108 · ClinicalTrials.gov registry record

Monitoring Biomarker for Detecting Change in Physical Activity and Limb Function in Inclusion Body Myositis Over Time

A clinical trial of Inclusion Body Myositis, sponsored by University of Kansas Medical Center.

Active
Registry status
20
Enrollment target
1
Study location

NCT06153108 is a study of Inclusion Body Myositis that is active but no longer recruiting, run by University of Kansas Medical Center. The registered enrollment target is 20 participants, below the 234-participant average among 10 other Inclusion Body Myositis trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06153108, a study of Inclusion Body Myositis, is active but no longer recruiting, sponsored by University of Kansas Medical Center.

ACTIVE NOT RECRUITING
Registry status
20 participants
Enrollment target
1
Study location

Study Summary

Inclusion-Body Myositis (IBM) results in weakness and the deterioration of distal arm muscles, the symptoms of which are currently assessed through expert examination at clinical visits. Such in-clinic assessments are time-consuming, subjective, of limited sensitivity, and only provide a snapshot of a patient's disease. In this project, the investigators will conduct clinical validation of monitoring digital biomarkers of upper limb function during activities of daily living using a wearable sensor platform that enables frequent, at-home monitoring of upper limb function health in IBM and could be incorporated into IBM trials.

Conditions Studied

Interventions

  • DEVICE PAMSys pendant PAMSys wrist sensors

Study Locations (1)

Kansas

  • University of Kansas Medical Center - Kansas City

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-11-16
Est. Completion 2027-12

Sponsor

University of Kansas Medical Center

408 total trials

What the Registry Record Tells You About NCT06153108

The ClinicalTrials.gov registry entry for NCT06153108 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 234-participant average among 10 other Inclusion Body Myositis trials with a reported enrollment target (91% lower). The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Inclusion Body Myositis appearing as the primary indexed condition, and to 1 intervention - of which PAMSys pendant PAMSys wrist sensors is the first listed.

NCT06153108 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.

Frequently Asked Questions

What is clinical trial NCT06153108 about?

NCT06153108 is a clinical study titled "Monitoring Biomarker for Detecting Change in Physical Activity and Limb Function in Inclusion Body Myositis Over Time". Inclusion-Body Myositis (IBM) results in weakness and the deterioration of distal arm muscles, the symptoms of which are currently assessed through expert examination at clinical visits. Such in-clinic assessments are time-consuming, subjective, of limited sensitivity, and only provide a snapshot of...

What is the current status of trial NCT06153108?

This trial is currently active not recruiting. The enrollment target is 20 participants. The study started on 2023-11-16. Estimated completion is 2027-12.

What conditions does trial NCT06153108 study?

This clinical trial studies the following conditions: Inclusion Body Myositis.

What interventions are being tested in trial NCT06153108?

The interventions under investigation include: PAMSys pendant PAMSys wrist sensors (DEVICE).

Who is sponsoring clinical trial NCT06153108?

This trial is sponsored by University of Kansas Medical Center, which has 408 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06153108 being conducted?

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

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

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