Massage Therapy After Thoracic or Lumbar Surgery

Description

The purpose of this research is to look at the effect of massage therapy on the pain, anxiety, and quality of life that pediatric patients have after undergoing spinal fusion surgery. This is a single-site, prospective, randomized, interventional study design that will involve post-thoracic and post-lumbar spinal fusion surgeries of pediatric patients from 7 to 19 years of age that present to Cook Children's Medical Center in Fort Worth, Texas. These patients will be identified prior to their scheduled spinal fusion surgery and recruited to enroll in the study. The planned spinal fusion surgeries are not considered part of this research project, but rather considered standard of care and would occur whether the patient is enrolled in this project or not. Enrolled participants will be followed during their inpatient stay and through their subsequent follow-up visits at weeks 2, 6, and 12. Participants will be randomly assigned to either a massage therapy group or a group that receives the standard (normal) care for recovery after surgery. The final study involvement will occur at week 16 (post-hospital discharge) where a study team member will administer a quality of life (PedsQL) questionnaire via phone or mail with the subject. Data will be collected after study related procedures are completed.

Conditions

Scoliosis; Adolescence, Adolescent Idiopathic Scoliosis, Thoracic Region, Adolescent Idiopathic Scoliosis, Lumbar Region

Study Overview

Study Details

Study overview

The purpose of this research is to look at the effect of massage therapy on the pain, anxiety, and quality of life that pediatric patients have after undergoing spinal fusion surgery. This is a single-site, prospective, randomized, interventional study design that will involve post-thoracic and post-lumbar spinal fusion surgeries of pediatric patients from 7 to 19 years of age that present to Cook Children's Medical Center in Fort Worth, Texas. These patients will be identified prior to their scheduled spinal fusion surgery and recruited to enroll in the study. The planned spinal fusion surgeries are not considered part of this research project, but rather considered standard of care and would occur whether the patient is enrolled in this project or not. Enrolled participants will be followed during their inpatient stay and through their subsequent follow-up visits at weeks 2, 6, and 12. Participants will be randomly assigned to either a massage therapy group or a group that receives the standard (normal) care for recovery after surgery. The final study involvement will occur at week 16 (post-hospital discharge) where a study team member will administer a quality of life (PedsQL) questionnaire via phone or mail with the subject. Data will be collected after study related procedures are completed.

The Impact of Massage Therapy on Post-Surgical Pain, Anxiety, Quality of Life, and Opioid Analgesia Exposure on Children After Thoracic or Lumbar Surgery

Massage Therapy After Thoracic or Lumbar Surgery

Condition
Scoliosis; Adolescence
Intervention / Treatment

-

Contacts and Locations

Fort Worth

Cook Children's Medical Center, Fort Worth, Texas, United States, 76104

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patients scheduled to undergo their first thoracic or lumbar spinal fusion surgery
  • * Able to participate and perform in a massage therapy as a recovery option
  • * Participant needs to be verbal
  • * Ability to understand study procedures and to comply with them for the entire length of the study
  • * Prospective patients scheduled to undergo any spinal fusion other than a thoracic or lumbar spinal fusion surgery.
  • * Prospective patients scheduled to undergo a second or multiple thoracic or lumbar spinal fusion surgery
  • * Previous cardiac surgery
  • * Chronic pain syndromes
  • * Chronic opioid usage
  • * History of psychosis
  • * Prolonged bleeding
  • * Intubation greater than 24 hours
  • * Illicit/recreation drug use
  • * Paralysis diagnosis
  • * History of chronic pain requiring medical intervention
  • * Neuromuscular scoliosis diagnosis
  • * Cerebral palsy diagnosis
  • * Developmental delay characteristics

Ages Eligible for Study

7 Years to 19 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Cook Children's Health Care System,

Meredith Brooks, MD, PRINCIPAL_INVESTIGATOR, Cook Children's Health Care System

Study Record Dates

2026-08-01