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In typical clinical conditions, patients with RM experience muscular weakness, myalgia, swelling, tenderness or stiffness and dark brown urine [ 1].
The study will add valuable information to the body of evidence relating to how women who have suffered RM experience the waiting period of a new pregnancy.
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To enhance coherence in the cancer survivors rehabilitation process the RMs experienced that a minimum of three rehabilitation in-person meetings was required.
This period, however, is likely to be relatively short, as many women who experience RM become pregnant quickly and have a short 'time-to-pregnancy', 26 despite difficulty carrying the pregnancy to term.
This research will involve a potentially vulnerable patient group that has experienced RM.
Additionally, the evaluation of the acceptability and feasibility of the PRCI will explore and identify how women who have experienced RM utilise this type of self-administered tool.
For women who have experienced RM, the waiting period in the early stages of pregnancy shares many characteristics and stress factors with the waiting period after fertility treatment.
This proposed randomised controlled trial (RCT) feasibility and acceptability study of the intervention is the next step in assessing the suitability of the PRCI as a coping intervention for women who have experienced RM.
As such, it is envisaged that this research will both enhance and complement ongoing studies within a wider programme of research into the care and management of women who experience RMs.
A mixed-method, two-centre, randomised controlled feasibility study aims to establish the viability of conducting a multicentre RCT to definitively test the effects of the PRCI on the psychological well-being of women who have experienced RM during the initial waiting period (1 12 weeks) of a subsequent pregnancy.
A randomised controlled trial (RCT) feasibility study will establish the viability of conducting a multicentre RCT to definitively test the effects of the PRCI on the psychological well-being of women who have experienced RM during the initial waiting period of a subsequent pregnancy.
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