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Table 2 Summary of outcome measures

From: BetaMe: impact of a comprehensive digital health programme on HbA1c and weight at 12 months for people with diabetes and pre-diabetes: study protocol for a randomised controlled trial

Outcomes

Time pointa

Measurement/definition

Primary outcome measures

 Change in HbA1c

At 12 months

Measured using whole blood sample collected in EDTA tube (2 ml minimum) using Variant Turbo Ion Exchange HPLC. Participants will either have a blood sample taken by the research nurse, or will be provided with a laboratory request form for an HbA1c blood test that will be taken as per usual processes within a week of the assessment period.

 Change in weight

At 12 months

Measured in kilograms using calibrated digital scales and standardised methods

Secondary outcome measures

 Change in HbA1c

At 4 months

Measured using whole blood sample collected in EDTA tube (2 ml minimum) using Variant Turbo Ion Exchange HPLC (as above)

 Change in weight

At 4 months

Measured in kilograms using calibrated digital scales and standardised methods

 Change in waist circumference

At 4 and 12 months

Measured in millimetres using tape measure using standardised methods

 Change in blood pressure

At 4 and 12 months

Measured using a calibrated syphgmomanometer using a standard approach (blood pressure taken when participant has been sitting quietly for 5 min, without eating, drinking or smoking. They will be asked to have feet flat on the floor, with their back up against the back of the chair, and their left arm straight on the table). Three measures will be taken with the lowest of the last two measures recorded

 Change in self-management

At 4 and 12 months

Measured using the Partners in Health Scale [37]

 Change of score in diabetic-specific behaviours and outcomes

At 4 and 12 months

Measured using the Summary of Diabetes Self-Care Activities tool, which assess participants’ self-care activities [38]

 Health-related quality of life

At 4 and 12 months

Measured using the five-level EuroQol five dimensions questionnaire (EQ-5D-5 L)

 Change in score of diabetes-specific outcomes

At 4 and 12 months

Measured using the Diabetes Distress Scale [39]

 Change in dose of insulin

At 4 months relative to baseline, and 12 months relative to 4 months

Categorised as (1) starting insulin in current time period; (2) increasing dose of insulin in current period; (3) reducing dose of insulin in current period or (4) stopping insulin in current period. Data will be collected from patients, verified where possible from clinic records

 Change in dose of metformin

At 4 months relative to baseline, and 12 months relative to 4 months

Categorised as (1) starting metformin in current time period; (2) increasing dose of metformin in current period; (3) reducing dose of metformin in current period or (4) stopping metformin in current period. Data will be collected from patients, verified where possible from clinic records

 Change in dose of other oral hypoglycaemic agents (not metformin)

At 4 months relative to baseline, and 12 months relative to 4 months

Categorised as (1) starting oral hypoglycaemic agents in current time period; (2) increasing dose of oral hypoglycaemic agents in current period; (3) reducing dose of oral hypoglycaemic agents in current period or (4) stopping oral hypoglycaemic agents in current period. Data will be collected from patients, verified where possible from clinic records

  1. EDTA ethylenediaminetetracetic acid, HbA1c glycosylated haemoglobin, HPLC high-performance liquid chromatography
  2. aAll time periods are time after recruitment, and compared with baseline with exception of changes in medication dose specified above