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Improving self-awareness in people with brain injury using video-feedback: A double-blinded randomised controlled trial

Improving self-awareness in people with brain injury using video-feedback: A double-blinded randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000378224
Enrollment
54
Registered
2009-05-28
Start date
2009-06-01
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

Main Objective: To determine the effectiveness of video feedback in improving on-line awareness and adjustment in persons with traumatic brain injury compared to verbal feedback and experiential feedback only. Hypothesis: 1. Treatment Group A (video & verbal feedback) & Treatment Group B (verbal feedback) will demonstrate greater improvement in on-line awareness compared to the control (experiential feedback) group. 2. Treatment Group A (video & verbal feedback) will demonstrate greater improvement in on-line awareness than Treatment Group B (verbal feedback). 3. Gains in on-line awareness will be maintained for Treatment Group A (video & verbal feedback) at four-week follow-up. 4. No hypotheses have been generated about the impact of the treatment on measures of intellectual awareness (AQ) or emotional status (DASS), as these are exploratory variables.

Interventions

Group 1: Verbal and video-tape feedback after the client completes a functional task. The participant and the therapist will watch the video of their functional task completion, and rate the client's performance using a standard rating form. This group will complete four intervention sessions of an hour's length, held within 4-6 weeks. The functional task is a hot meal preparation, with the participant's choice of spaghetti bolognaise or pizza.

Sponsors

Royal Rehab Centre, Sydney
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

-Diagnosis of a traumatic brain injury -At least 18 years old -Emerged from post-traumatic amnesia (PTA) to allow for informed consent and ensure participants can recall feedback -Functional in the English language to maximise comprehension of information -Difference in two scores between the therapist and the participant on the Awareness Questionnaire indicating impaired self-awareness. Provides informed consent to participate in the study

Exclusion criteria

-Severe communication disability or behavioural changes that would compromise ability to participate in an intervention -Expected length of rehabilitation less than intervention study period (i.e. two weeks)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026