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Table 3 Characteristics of participants

From: Strategies to optimise the health equity impact of digital pain self-reporting tools: a series of multi-stakeholder focus groups

Characteristics of focus groups participants (n = 28)

Characteristics

Categories

Number (percentage)

People living with musculoskeletal pain conditions (n = 15)

 Age

44 and younger

4 (27)

45—64

5 (33)

65 and older

6 (40)

 Gender

Male

8 (53)

Female

7 (47)

 Ethnicity

White

9 (60)

Asian or Asian British

4 (27)

Black African/Caribbean

2 (13)

 Socio-economic status

IMD; decile 1–3; most deprived

7 (46)

IMD; decile 4–6;

4 (27)

IMD; decile 7–10; least deprived

4 (27)

 Employment status

Employed (full or part)

7 (47)

Not working (unemployed; retired)

8 (53)

 Number of musculoskeletal conditions

One

13 (87)

Two or more

2 (13)

 Number of other long-term conditions

1–2

9 (60)

3 or more

6 (40)

 Experience living with pain

1 to 3 years

6 (40)

4 to 10 years

5 (33)

More than 10 years

4 (27)

Professionals with domain expertise (n = 13)

 Age

25 – 44

8 (62)

45—64

5 (38)

 Gender

Male

6 (46)

Female

7 (54)

 Ethnicity

White

10 (77)

Asian or Asian British

2 (15)

Mixed/multiple ethnic group

1 (8)

 Main profession/domain of expertise

Chronic pain researcher/expert

3 (23)

Healthcare professional

3 (23)

Technology researcher/developer

4 (31)

Other

3 (23)

 Years of professional experience

Less than a year

3 (23)

4—10 years

6 (46)

More than 10 years

4 (31)

  1. Abbreviations: IMD Index of Multiple Deprivation, which is a relative measure of deprivation across small areas in the UK. The IMD is calculated based on socio-economic factors and living conditions. IMD deciles are constructed by ranking all small areas from most deprived to least deprived and dividing them into 10 equal groups [51]