SUSPENDED

Posture Correction in Cubital Tunnel Syndrome

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary objective of this study is to determine whether the UpRight Go posture trainer reduces the symptoms of cubital tunnel syndrome in patients who have not had corrective surgery, as determined by improvements in VAS scores for pain, numbness, and weakness.

Official Title

Posture Correction for the Treatment of Cubital Tunnel Syndrome (CuTS)

Quick Facts

Study Start:2023-12-15

Study Completion:2025-12

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:SUSPENDED

Study ID

NCT06095011

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Adult patients, between 18 and 99 years old * Exhibiting signs and symptoms consistent with cubital tunnel syndrome including but not limited to pain, numbness, or paresthesia in an ulnar distribution, loss of grip strength, or loss of fine motor control of the fingers. * Nerve conduction study, electromyography, MRI or ultrasound results consistent with the diagnosis of cubital tunnel syndrome * Ability to wear a posture trainer daily and manage the associated smartphone application and questionnaire	* History of spinal surgery, hand surgery or hand/wrist fracture * History of cubital tunnel release surgery or carpal tunnel syndrome * Pregnancy or lactation * Known allergic reactions to silicon * Long-standing history of T2DM, documented neuropathic pain

Inclusion Criteria

Exclusion Criteria

* Provision of signed and dated informed consent form
* Stated willingness to comply with all study procedures and availability for the duration of the study
* Adult patients, between 18 and 99 years old
* Exhibiting signs and symptoms consistent with cubital tunnel syndrome including but not limited to pain, numbness, or paresthesia in an ulnar distribution, loss of grip strength, or loss of fine motor control of the fingers.
* Nerve conduction study, electromyography, MRI or ultrasound results consistent with the diagnosis of cubital tunnel syndrome
* Ability to wear a posture trainer daily and manage the associated smartphone application and questionnaire

* History of spinal surgery, hand surgery or hand/wrist fracture
* History of cubital tunnel release surgery or carpal tunnel syndrome
* Pregnancy or lactation
* Known allergic reactions to silicon
* Long-standing history of T2DM, documented neuropathic pain

Contacts and Locations

Principal Investigator

Elspeth Hill, MBChB, PhD, MRes, MRCS

PRINCIPAL_INVESTIGATOR

Yale University

Study Locations (Sites)

Yale New Haven Hospital

New Haven, Connecticut, 06520

United States

Collaborators and Investigators

Sponsor: Yale University

Elspeth Hill, MBChB, PhD, MRes, MRCS, PRINCIPAL_INVESTIGATOR, Yale University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-15

Study Completion Date2025-12

Study Record Updates

Study Start Date2023-12-15

Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

Cubital Tunnel Syndrome