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Clinical Trials/NCT01463930
NCT01463930CompletedNot Applicable

Effects of an Educational Audiovisual Videodisc on Patients' Pre-operative Expectations With Total Knee Replacement: a Randomized Study

Parc de Salut Mar2 sites in 1 country92 target enrollmentStarted: January 1, 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
92
Locations
2
Primary Endpoint
Change from baseline in patient-reported postoperative expectatives about the results of total knee replacement to inmediately after receiving audiovisual plus verbal information (intervention grou) or only verbal information (control group)

Study Overview

Brief Summary

Information provided to patients modifies their expectations with surgery. The effects of preoperative audiovisual information on expectations with total knee replacement (TKR) have not been investigated. The purposes of this study were to investigate the effectiveness of an educational videodisc on the modification of pre-operative patients' expectations with TKR and to find a biophysical profile of subjects in whom this videodisc could be most effective. It was hypothesized that patients receiving standard information plus additional medical information through audiovisual videodiscs would modify their pre-operative expectations more than those only receiving the standard information through medical interviews.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with knee osteoarthritis waiting for total knee replacement.

Exclusion Criteria

  • Cognitive disorders or language barriers precluding medical interview.
  • Contralateral total knee replacement.
  • History of revision total knee replacement.
  • History of unicompartmental knee arthroplasty

Outcomes

Primary Outcomes

Change from baseline in patient-reported postoperative expectatives about the results of total knee replacement to inmediately after receiving audiovisual plus verbal information (intervention grou) or only verbal information (control group)

Time Frame: Baseline and 1 month later (1 month before surgery)

The study measures the patient's expectatives about the improvement of pain, function, and psychological well-being after undergoing total knee replacement. These expectatives are measured through the Hospital for Special Surgery Knee Replacement Expectations Survey (KRES), and a score ranging from 0 to 100 is reported.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Parc de Salut Mar
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Joan Leal Blanquet

MD, MSc, PhD

Parc de Salut Mar

Study Sites (2)

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