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Answers were recorded on a 5 point Likert scale where the lower number represents a better outcome.\n\nScale descriptors:\n\nQ1 (Overall Experience): 1 (Very comfortable)/ 2 (Comfortable)/ 3 (Neither comfortable or uncomfortable)/ 4 (Uncomfortable)/ 5 (Very uncomfortable) Q2 (Adverse Effects): 1 (YES) / 0 (NO) Q3 (Length of Time): 0 (Too short) / 1 (Just right) / 2 (Too long) Q4 (Pain/Discomfort): 1 (No Increase)/ 2 (Mild Increase)/ 3 (Moderate Increase)/ 4 (High Increase)/ 5 (Severe Increase) Q5 (Likely to Reparticipate): 0 (Extremely Unlikely) / 1 (Unlikely) / 2 (Neither Likely or Unlikely) / 3 (Likely) / 4 (Extremely Likely) Q6 (How similar to expectations): 1 (YES) / 0 (NO) Q7 (Comfort with Staff): 1 (YES) / 0 (NO)","dispersionType":"Standard Deviation","groups":[{"description":"Participants recruited with myeloma","id":"OG000","title":"Group 1- Myeloma"},{"description":"Participants recruited with MGUS","id":"OG001","title":"Group 2- MGUS"},{"description":"Participants recruited as healthy volunteers","id":"OG002","title":"Group 3- Healthy Volunteers"}],"paramType":"MEAN","populationDescription":"Baseline: all participants from Groups 1,2,3 were invited for novel MR scan, and only participants from Groups 1 and 2 were invited for DXA Follow-up: only participants from Groups 1 and 2 were invited for a novel MR scan and also a DXA.","reportingStatus":"POSTED","timeFrame":"At baseline and six months","title":"Secondary Outcome 4: Assess Participants' Experience of Novel Magnetic Resonance (MR) and Dual-energy X-ray Absorptiometry (DXA) Scans","type":"SECONDARY","unitOfMeasure":"Score on a scale (see description above)"}