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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03513120
Other study ID # 17-2473
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 8, 2018
Est. completion date August 31, 2020

Study information

Verified date December 2020
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary purpose of this prospective study is to determine when adolescent athletes with idiopathic scoliosis are able to return to sports participation after posterior spinal fusion surgery.


Description:

The investigators aim to determine at what time subjects return to athletic activity, and how long after surgery they are performing at pre-surgical levels. The investigators will enroll adolescent athletes that meet the inclusion criteria below, and follow their postoperative activity level with standardized activity questionnaires on a monthly basis until the subject reaches their baseline pre-surgical performance level. The investigators primary aim is to determine at what time patients return to sports without any restrictions to contact level or type of play. The investigators secondary aim is to quantitatively assess when patients are able to compete at their prior level of play as determined by self-assessment surveys, as well as identify any post-operative complications in these patients after return to sports.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date August 31, 2020
Est. primary completion date August 31, 2020
Accepts healthy volunteers No
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria: - Level of play: high school or club level - Frequency of play at above level: >3mos/year - Age: 10-18 years of age (inclusive) - Sports: at least one sport, contact, non-contact, or collision. No sports exclusion criteria - Spinal deformity criteria: Adolescent idiopathic scoliosis, curve size 40-75 degrees Exclusion Criteria: - Play at recreational/intramural level - Non-English Speaking Patient - Sports participation <3 mos/year - Non idiopathic etiology or curves >75 degrees - Treatment outside of Children's Hospital Colorado provider care network

Study Design


Locations

Country Name City State
United States Children's Hospital Colorado Aurora Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Return to Sport Identify at what time patients return to sports without any restrictions. Less than 1 year following surgery
Secondary Physical Function Levels Identify at what time patients report physical function returns to their pre-surgical levels. Less than 1 year following surgery
Secondary Postoperative Complications Identify any postoperative complications related to release to full activity one month after surgery. Up to 1 year follow up
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