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Biopsychosocial Impact on Caregivers in Patients Undergoing Joint and Spine Surgery

Pain, Postoperative Clinical Trial

Official title:
Characterizing the Biopsychosocial Impact on Caregivers in Patients Undergoing Joint Replacement and Cervical/Thoracic/Lumbar Spine Surgery: A Pilot Study

Clinical Trial Summary

The purpose of this study is to describe the biopsychosocial impact of caregivers in patients undergoing total knee arthroplasty, total hip arthroplasty, and cervical/thoracic/lumbar spine surgery.Defining such impacts may offer opportunities to enhance caregiver capability to provide care following surgery on a loved one.

Clinical Trial Description

This is a pilot feasibility study with the goal of enrolling 50 caregivers in each surgical subgroup, with a total of 150 subjects. Caregivers for patients undergoing the above surgeries will be administered Patient Reported Outcome Measurement Information System (PROMIS) measures preoperatively, 7 days postoperatively, 14 days postoperatively, and 1 month postoperatively. PROMIS item banks will include Global Health, Anxiety, Fatigue, Depression, Self Efficacy, Social Satisfaction, and Sleep Disturbance. If the caregiver reports the presence of persistent pain, Pain Interference and Physical Function will be administered. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03059602
Study type Observational
Source Defense and Veterans Center for Integrative Pain Management
Contact
Status Completed
Phase
Start date May 12, 2016
Completion date October 30, 2018
View Details
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