RECRUITING

Impact of a Telerehabilitation Program With Technology Enhancement on Post-burn Recovery

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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 purpose of this study is to examine the effect of participating in a tele-rehabilitation program after a burn.

Official Title

Impact of a Telerehabilitation Program With Technology Enhancement on Post-burn Recovery

Quick Facts

Study Start:2024-04

Study Completion:2024-09

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06162052

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 to 79 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Adults: ≥18 to ≤79 years of age * Not participating in another interventional trial * Admitted to the Blocker Burn Unit for treatment of initial burn * Subject is able and willing to follow the protocol requirements * Burn wound / scar / contracture occurring across at least one joint. * Has regular access to smart phone, tablet, or computer with internet access.	* Any medical condition that, in the opinion of the investigator or physician, would place the subject at increased risk for participation. * Concurrent participation on another interventional clinical trial * History of prior non-compliance or the presence or history of psychiatric condition (including drug or alcohol addiction) that would, in the opinion of the investigator, make it difficult for the subject to comply with the study procedures or follow the investigators instructions. * Patients without internet access.

Inclusion Criteria

Exclusion Criteria

* Adults: ≥18 to ≤79 years of age
* Not participating in another interventional trial
* Admitted to the Blocker Burn Unit for treatment of initial burn
* Subject is able and willing to follow the protocol requirements
* Burn wound / scar / contracture occurring across at least one joint.
* Has regular access to smart phone, tablet, or computer with internet access.

* Any medical condition that, in the opinion of the investigator or physician, would place the subject at increased risk for participation.
* Concurrent participation on another interventional clinical trial
* History of prior non-compliance or the presence or history of psychiatric condition (including drug or alcohol addiction) that would, in the opinion of the investigator, make it difficult for the subject to comply with the study procedures or follow the investigators instructions.
* Patients without internet access.

Contacts and Locations

Study Contact

Celeste Finnerty, PhD

CONTACT

(409)772-1011

ccfinner@utmb.edu

Steven E. Wolf, MD

CONTACT

(409)772-1011

swolf@utmb.edu

Principal Investigator

Celeste Finnerty, PhD

PRINCIPAL_INVESTIGATOR

University of Texas

Study Locations (Sites)

University of Texas Medical Branch

Galveston, Texas, 77555

United States

Collaborators and Investigators

Sponsor: The University of Texas Medical Branch, Galveston

Celeste Finnerty, PhD, PRINCIPAL_INVESTIGATOR, University of Texas

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 Date2024-04

Study Completion Date2024-09

Study Record Updates

Study Start Date2024-04

Study Completion Date2024-09

Terms related to this study

Additional Relevant MeSH Terms

Burns