Psychological Assessment of Scoliosis Patients Undergoing Surgical Management (PASS)

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Working in partnership with Montefiore-Einstein's Department of Translational Psychiatry, the study team investigators have designed a prospective randomized clinical trial (2:1) study for 45 AIS patients (10-19 yrs.). This protocol includes a baseline assessment of mental health, pain, and function in AIS patients utilizing validated patient reported outcome measures. The investigators will implement and test a structured perioperative psychological intervention program, based on the Aim to Decrease Anxiety and Pain Treatment (ADAPT), which was developed based on evidence-based cognitive behavioral therapy (CBT) protocols for the management of pediatric pain and childhood anxiety disorders

Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 19
Healthy Volunteers: f
View:

• Diagnosis of scoliosis prior to age 20

• Healthy, non-obese aged 10-19 years, with a diagnosis of idiopathic scoliosis, undergoing elective posterior spinal fusion

Locations
United States
New York
Montefiore Medical Center
RECRUITING
The Bronx
Contact Information
Primary
Leila Mehraban Alvandi, PhD
lalvandi@montefiore.org
347-419-4226
Backup
Eric Fornari, MD
EFORNARI@montefiore.org
718-920-5532
Time Frame
Start Date: 2023-10-06
Estimated Completion Date: 2026-10
Participants
Target number of participants: 120
Treatments
No_intervention: standard of care control groups no psychological intervention
standard of care control groups no psychological intervention
Experimental: psychological intervention ADAPT
The psychological intervention plan is based on the Aim to Decrease Anxiety and Pain Treatment (ADAPT) model.
Related Therapeutic Areas
Sponsors
Collaborators: Albert Einstein College of Medicine
Leads: Montefiore Medical Center

This content was sourced from clinicaltrials.gov