Butzon 1997.
Methods | Quasi‐randomised cross‐over study | |
Participants | 24 presbyopic volunteers from research and development personnel of a telecommunications equipment company who were age 47 or older wearing a full‐time multifocal lens design, needing a near add power of at least S+1.50 dioptres, that worked at a computer for 4 hours per day or more. Mean age: 53 years, range 47 to 66 Male/Female: 19/5 Mean time spent at a VDT per day: at least 4 hours (type of computer not described) Refractive error: not described, near add power of at least S+1.50 dioptres Country: USA |
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Interventions | Eyeglasses: progressive computer glasses (Technica by American Optical) vs. trifocal computer glasses (Datalite CRT trifocal by Vision‐Ease); each type of eyeglasses was worn for a period of 3 weeks, followed by a direct comparison during 3 weeks | |
Outcomes | Frequency and severity of symptoms at baseline and after each intervention period (3 and 6 weeks). Wearing time of the eyeglasses expressed as % of the working day. | |
Notes | Authors did not respond to our request for information about the allocation method. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | Intervention and comparison in "counterbalanced order". |
Allocation concealment (selection bias) | Unclear risk | Intervention and comparison in a "counterbalanced order"; no attempt to concealment reported. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Blinding not possible because of differences in visual aspect of the eyeglasses: progressive vs. trifocal. |
Blinding of outcome assessment (detection bias) Primary outcomes | High risk | No blinding of outcome assessment, as participants are outcome assessors. |
Blinding of outcome assessment (detection bias) Secondary outcomes | High risk | No blinding of outcome assessment, as participants are outcome assessors. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | 24 participants who all completed the study and answered all questionnaires. |
Selective reporting (reporting bias) | Unclear risk | No study protocol. All outcomes mentioned in the methods section are reported. |
Other bias | High risk | No wash‐out period between interventions. |