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Pilot study to assess the feasibility and patient numbers required prior to a randomised controlled trial of the effect of visual distraction for painful procedures in the burns unit

Pilot study to assess the feasibility and patient numbers required prior to a randomised controlled trial of the effect of visual distraction for painful procedures in the burns unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN69643568
Enrollment
10
Registered
2004-09-30
Start date
2003-04-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Pain Injury, Occupational Diseases, Poisoning Burn and corrosion, body region unspecified

Interventions

Short visual analogue scale patient rated scores for pain and anxiety, an appropriate questionnaire and short concluding taped interview after intervention. Quantitative methods will be used.

Sponsors

Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Minimum 10 consenting adults suitable to trial criteria and protocols.

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Improved pain control and toleration of regular dressing change and debridement of burns with reduced anxiety and awareness.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026