Cognitive Behavioural Therapy to Optimize Post-Operative Recovery Trial

NACompletedINTERVENTIONAL
Enrollment

1,024

Participants

Timeline

Start Date

January 25, 2021

Primary Completion Date

August 18, 2025

Study Completion Date

August 18, 2025

Conditions
Pain, PostoperativePain, AcutePain, ChronicFractures, ClosedFractures, Open
Interventions
BEHAVIORAL

Cognitive Behavioural Therapy

Participants who are randomized to the CBT intervention will be encouraged to begin CBT immediately following randomization. The CBT intervention will focus on addressing maladaptive beliefs related to pain and recovery as well as teaching skills to enhance coping and management of pain symptoms. The specific focus of CBT sessions will be informed by each individual patient's responses to baseline questionnaires. All other aspects of post-operative care will be at the discretion of participant's surgeon.

Trial Locations (10)

20774

University of Maryland - Capital Region Medical Center, Largo

21201

University of Maryland - R Adams Cowley Shock Trauma Center, Baltimore

29615

PRISMA Health, Greenwood

46202

Indiana University Health Methodist Hospital, Indianapolis

02215

Beth Israel Deaconess Medical Centre, Boston

03766

Dartmouth-Hitchcock Medical Centre, Lebanon

Unknown

University of Calgary - Foothills Hospital, Calgary

Memorial University Newfoundland, St. John's

Ottawa Civic Hospital, Ottawa

L8L 2X2

Hamilton Health Sciences - General Site, Hamilton

All Listed Sponsors
collaborator

Orthopaedic Trauma Association

OTHER

collaborator

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

lead

McMaster University

OTHER

NCT04274530 - Cognitive Behavioural Therapy to Optimize Post-Operative Recovery Trial | Biotech Hunter | Biotech Hunter