Taaffe 1999.
Methods | Type of study: RCT | |
Participants | Number of participants randomised: 46 Losses:7 (5 in exercise and 2 control) N = 46 Age: 65 to 79 years Sex: 29 males, 17 females Health status as defined by authors: healthy Residential status of participants: community dwellers Setting: USA Inclusion: BMI < 30 Kg/m2 Exclusion: musculoskeletal disorders inhibiting exercise, participation in weight training in past 12 months |
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Interventions | EXERCISE GROUP (STRENGTH): high intensity progressive resistance training at 80% of 1 RM (repetition maximum) (repetition maximum) for upper and lower limbs. CONTROL GROUP: usual activity Duration and intensity: Ex1 = 1 day per week for 24 weeks, Ex2 = 2 days per week for 24 weeks, Ex3 = 3 days per week for 24 weeks Supervisor: not stated Supervision: group with direct supervision Setting: gym | |
Outcomes | backward tandem walk over 6 m Compliance/adherence: similar across interventions Adverse events: not reported |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Insufficient information to permit judgement |
Allocation concealment (selection bias) | Unclear risk | Insufficient information to permit judgement |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Insufficient reporting of attrition/exclusions to permit judgement |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to permit judgement |
Other bias | Low risk | The study appears to be free of other sources of bias |
Blinding (participant) | High risk | Not possible |
Blinding (assessor) | Unclear risk | Insufficient information to permit judgement |
Were the treatment and control group comparable at entry? | Low risk | No differences reported on baseline characteristics with a potential to influence the effect of the intervention |
Was the surveillance active, and of clinically appropriate duration (i.e. at least 3 months post intervention)? | High risk | Only immediately post intervention data, no follow‐up data reported. |