Abrams 1992.
Methods | Randomised trial (also had a control group with no intervention but control group inclusion was determined by eligibility for VA‐funded HA so not randomised) | |
Participants | N = 22 in randomised groups Age: 55 and over, PTA 4 frequency average > 30 dB HL in better ear, no previous HA use, women not excluded but none in study Excluded known neurological deficiencies |
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Interventions | HA + AR group programme versus HA alone AR programme was 90‐minute group session once a week for 3 weeks post‐fitting |
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Outcomes | Short‐term: baseline and 2 months HANDICAP Hearing Handicap Inventory for the Elderly (HHIE) total score, emotional subscale and social subscale |
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Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "those who received hearing aids were randomly assigned to one of the two treatment groups" Comment: no details given about how sequence was generated Control group not randomised |
Allocation concealment (selection bias) | Unclear risk | Comment: no information about how sequence generated or whether it was concealed |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Comment: participants not blinded (due to the nature of the intervention) and experimenters almost certainly not, but it was not explicitly stated in the text |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Not blinded |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Comment: no missing data |
Selective reporting (reporting bias) | Unclear risk | No study protocol available |
Other bias | Low risk | Study appears to be free of other sources of bias |