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Using multimedia to enhance patient education when obtaining informed consent in an orthopaedic foot and ankle practice

To determine the efficacy of the use of multimedia patient education technology when obtaining informed consent in an orthopaedic foot and ankle practice.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000080820
Acronym
Nil
Enrollment
500
Registered
2012-01-16
Start date
2012-03-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

We hypothesise that multimedia patient education technology is superior to the traditional surgeon patient verbal process of obtaining informed consent for a variety of orthopaedic procedures including lateral ligament reconstruction, hallux valgus deformity correction, first metatarsal phalangeal fusion, Morton’s neuroma resection, and ankle arthroscopy.

Interventions

Patients participating in the study will be given the opportunity to watch a multimedia patient education module (approximately 20 minutes in length) on the surgical procedure applicable to their All patient will be asked to complete a knowledge questionnaire after a discussion with their treating surgeon. Patients participating in the trial will then be asked to watch the multi media which the risks and benefits of the surgical procedure applicable to their condition. They will then be asked

Patients participating in the study will be given the opportunity to watch a multimedia patient education module (approximately 20 minutes in length) on the surgical procedure applicable to their All patient will be asked to complete a knowledge questionnaire after a discussion with their treating surgeon. Patients participating in the trial will then be asked to watch the multi media which the risks and benefits of the surgical procedure applicable to their condition. They will then be asked to complete the same knowledge questionnaire. in order to obtain informed consent.

Sponsors

Epworth Foundation - Foot and Ankle Research Fund
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion Criteria Primary language is English Able to hear the spoken word Able to read English Has basic computer skills

Exclusion criteria

Exclusion criteria Unable to read Hearing impaired Non-English speaking Lacks basic computer skills

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026