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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05818969
Other study ID # 2.0 - 20203698
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date December 31, 2023

Study information

Verified date June 2024
Source Foundation for Orthopaedic Research and Education
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to collect information to evaluate the role of the psychogenic component of pain induced by anxiety on postoperative outcomes in major orthopaedic surgery and to determine whether hypnosis therapy provided during the perioperative period will lead to decreased use of opioid therapy. Patients are randomly assigned to one of two treatment groups: (I) usual care, or; (II) hypnotherapy treatment. Patients have an equal chance of being assigned to one of the two groups.


Recruitment information / eligibility

Status Completed
Enrollment 73
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of primary knee arthritis, in need of a total knee arthroplasty. - The ability to read, speak, and understand English - The ability and willingness to use a web-based application (OBERD) on a smartphone, pad/tablet, or computer - 18 years of age or older Exclusion Criteria: - Revision total knee arthroplasty - Any knee procedure except a primary knee arthroplasty, since these procedures have shown to result on increased postoperative pain compared to primary surgery - Patients with active cancer or receiving palliative care

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Hypnosis Therapy
Pre-recorded hypnosis therapy audio recording with accompanying visual of a calming ocean scene to be played at least once daily for 7 days preoperatively.

Locations

Country Name City State
United States Florida Orthopaedic Institute Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
Foundation for Orthopaedic Research and Education

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Perioperative Anxiety - Amsterdam Preoperative Anxiety and Information Scale (APAIS) Patient-reported anxiety in the perioperative period 7 days prior to surgery, 10 days postoperative day, 49 days postoperative day
Secondary Change in Perioperative Pain - Knee Society Score/ Knee Injury and Osteoarthritis Scores Patient-reported pain in the perioperative period 7 days prior to surgery, 10 days postoperative day, 49 days postoperative day
Secondary Change in Opioid Consumption - The Beliefs and Attitudes to Hypnosis Valencia Scale-Client Change in Anxiolytic Consumption 7 days prior to surgery, 10 days postoperative day, 49 days postoperative day
Secondary Change in Anxiolytic Consumption - The Beliefs and Attitudes to Hypnosis Valencia Scale-Client Change in Anxiolytic Consumption 7 days prior to surgery, 10 days postoperative day, 49 days postoperative day
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