Methods
Individuals with leg ulcers enrolled in a randomized controlled trial between 2004 and 2008 formed the study sample [29]. The primary outcome of the original study was
time to ulcer healing (fully epithelialized, no scab, no drainage), with pain and health-related quality of life (HRQL) as secondary outcomes. Healing measures were collected as close to the first observation of healing as possible, typically
the same day or the following visit. Baseline and healing assessment data from the trial formed the dataset for the current study. Ethics approval for the trial was received from Queen's University Research Ethics Board, Kingston, Ontario, Canada (REB# NURS-140-03).
Methods
Individuals with leg ulcers enrolled in a randomized controlled trial between 2004 and 2008 formed the study sample [29]. The primary outcome of the original study was
time to ulcer healing (fully epithelialized, no scab, no drainage), with pain and health-related quality of life (HRQL) as secondary outcomes. Healing measures were collected as close to the first observation of healing as possible, typically
the same day or the following visit. Baseline and healing assessment data from the trial formed the dataset for the current study. Ethics approval for the trial was received from Queen's University Research Ethics Board, Kingston, Ontario, Canada (REB# NURS-140-03).
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