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Factors that may hinder or facilitate the use of the intervention will be reviewed in the course of this project and strategies will be explored to positively affect intervention use.
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The intervention protocol will be detailed in a study manual, and a minimum of 20% of intervention sessions will be reviewed by an external reviewer to ensure adherence to the delivery of the intervention protocol.
Eligible patients will be invited to participate in the study and the medication of the patients listed in the intervention practices will be reviewed.
For the baseline measurement patient records of hip fracture patients acutely admitted in 2007, the year previous to the start of the intervention study, will be reviewed using a structured review form.
At these appointments intervention participants' mood will be reviewed, together with their current pharmacological and psychological treatments and any relevant social factors, with the nurse suggesting possible amendments according to evidence based guidelines.
In addition, the pros and cons of possible pharmacological interventions with Hippo signalling will be reviewed, with particular emphasis on anti-cancer drug development and regenerative medicine.
Recordings of the first 10 intervention sessions for each site will be reviewed by the research team for compliance.
Any woman in the intervention group who loses a cumulative 3 kg over the pregnancy will be reviewed by the Intervention Midwife and asked to complete a 7-day food diary to confirm that she is eating a healthy amount of food.
With the participants consent, each PST intervention will be taped and one third of randomly selected tape recordings will be reviewed to ensure the fidelity of the intervention.
The exercises will be reviewed, if necessary, after each session until the last week of intervention.
Specifically, all PST consultations will be taped and 1/3 of them will be reviewed by the research team to ensure the fidelity of this intervention.
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