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. 2021 Jan 13;12(4):1481–1499. doi: 10.1093/advances/nmaa157

TABLE 2.

Quality appraisals of studies in which the effects of CS, LNCS, and UNS preloads on energy intakes were assessed1

Reference Q1 Q2 Q3 Q5 Q6 Q7 Q8 Q9 Q102 Q113 Q12 Q13 Q14 Q15 Total, n (%)
Akhavan et al. (2011)—experiment 1 (31) Yes NR NR NR Yes NR NR Yes Yes Yes Yes Yes Yes Yes 9 (64)
Akhavan et al. (2011)—experiment 2 (31) Yes NR NR NR Yes NR NR Yes Yes Yes Yes Yes Yes Yes 9 (64)
Almiron-Roig and Drewnowski (2003) (32) No NR NR NR Yes Yes Yes Yes NA Yes Yes Yes Yes Yes 9 (69)
Anderson et al. (1989) (62) Yes NR NR Yes Yes Yes Yes Yes Yes Yes Yes NR Yes Yes 11 (79)
Anton et al. (2010) (33) No NR NR NR Yes Yes Yes Yes Yes NR Yes Yes Yes Yes 9 (64)
Bennett et al. (2018) (63) Yes NR NR NR Yes Yes Yes Yes Yes Yes Yes NR Yes Yes 10 (71)
Björvell and Rössner (1982) (34) Yes NR NR Yes Yes Yes Yes Yes NR NR Yes NR Yes Yes 9 (64)
Black et al. (1991) (35) Yes NR NR NR Yes NR NR Yes Yes NR Yes Yes Yes NR 7 (50)
Black et al. (1993) (36) Yes NR NR NR Yes NR NR Yes Yes NR Yes NR Yes NR 6 (43)
Canty and Chan (1991) (37) Yes NR NR Yes Yes NR NR Yes Yes NR Yes Yes Yes NR 8 (57)
Cuomo et al. (2011) (38) Yes NR NR Yes Yes NR NR Yes NA NR Yes Yes Yes NR 7 (54)
DellaValle et al. (2005) (39) No NR NR NR Yes Yes Yes Yes Yes Yes Yes NR Yes No 8 (57)
Drewnowski et al. (1994) (40) No NR NR NR Yes NR NR Yes NA NR Yes NR Yes NR 4 (31)
Drewnowski et al. (1994) (41) No NR NR NR Yes Yes Yes Yes NA NR Yes NR Yes Yes 7 (54)
Farhat et al. (2019) (42) Yes NR NR No Yes Yes Yes Yes Yes NR Yes Yes Yes Yes 10 (71)
Ford et al. (2011) (43) Yes NR NR No Yes Yes Yes Yes NR Yes Yes NR Yes Yes 9 (64)
Gadah et al. (2016) (44) Yes NR NR NR Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11 (79)
Hetherington et al. (2000)—exp 1 (64) No NR NR Yes Yes NR NR Yes NR Yes Yes NR Yes NR 6 (43)
Hetherington et al. (2000)—exp 2 (64) No NR NR NR Yes Yes Yes Yes NR Yes Yes NR Yes Yes 8 (57)
Kim (2006) (45) Yes NR NR NR Yes Yes Yes Yes NR Yes Yes NR Yes Yes 9 (64)
Lavin et al. (2002) (46) No NR NR NR Yes NR NR Yes NR NR Yes NR Yes NR 4 (29)
Maersk et al. (2012) (47) Yes NR NR NR Yes Yes Yes Yes NR Yes Yes Yes Yes Yes 10 (71)
Monsivais et al. (2007) (48) No NR NR NR Yes Yes Yes Yes NR NR Yes Yes Yes Yes 8 (57)
Poirier et al. (2019) (65) Yes NR NR NR Yes Yes Yes Yes NR Yes Yes NR Yes Yes 9 (64)
Ranawana and Henry (2010) (49) Yes NR NR No Yes Yes Yes Yes Yes Yes Yes NR Yes No 9 (64)
Rodin (1990) (50) Yes NR NR NR Yes Yes Yes Yes NR NR Yes NR Yes No 7 (50)
Rogers and Blundell (1989) (51) No NR NR Yes Yes Yes Yes Yes Yes NR Yes NR Yes No 8 (57)
Rogers et al. (1988) (52) No NR NR No Yes NR NR Yes Yes NR Yes NR Yes NR 5 (36)
Rogers et al. (1990)—exp 1 (53) No NR NR NR Yes NR NR Yes Yes NR Yes NR Yes NR 5 (36)
Rogers et al. (1990)—exp 2 (53) No NR NR Yes Yes NR NR Yes Yes NR Yes NR Yes NR 6 (43)
Rogers et al. (1991) (54) No NR NR Yes Yes NR NR Yes Yes NR Yes NR Yes NR 6 (43)
Rolls et al. (1990) (55) No NR NR NR Yes NR NR Yes NR NR Yes NR Yes NR 4 (29)
Shafer et al. (1987)—exp 1 (56) Yes NR NR Yes Yes NR NR Yes NR NR Yes NR Yes NR 6 (43)
Shafer et al. (1987)—exp 2 (56) No NR NR NR Yes NR NR Yes NR NR Yes NR Yes NR 4 (29)
Soenen and Westerterp-Platenga (2007) (57) Yes NR NR NR Yes Yes Yes Yes NA Yes Yes No Yes Yes 9 (69)
Stamataki et al. (2020) (58) Yes Yes Yes Yes Yes Yes Yes Yes Yes NR Yes Yes Yes Yes 13 (93)
Tey et al. (2017) (59) Yes NR NR Yes Yes Yes Yes Yes NR Yes Yes Yes Yes No 10 (71)
Vozzo et al. (2002)—exp 1 (60) Yes NR NR No Yes Yes Yes Yes NR Yes Yes NR Yes Yes 9 (64)
Vozzo et al. (2002)—exp 2 (60) Yes NR NR No Yes Yes Yes Yes NR Yes Yes NR Yes Yes 9 (64)
Woodend and Anderson (2001) (61) No NR NR NR Yes Yes Yes Yes NA NR Yes NR Yes No 6 (46)
Total, n (%) 23 (58) 1 (3) 1 (3) 11 (28) 40 (100) 24 (60) 24 (60) 40 (100) 18 (53) 18 (45) 40 (100) 13 (33) 40 (100) 20 (50)

1Questions were as follows: Q1. Was the study described as randomized, a randomized trial, a randomized clinical trial, or an RCT? Q2. Was the method of randomization adequate (i.e., use of randomly generated assignment)? Q3. Was the treatment allocation concealed (so that assignments could not be predicted)? Q4. Were study participants and providers blinded to treatment group assignment? [Omitted because of the nature of the studies and the challenges in blinding (participants can distinguish sweetened from unsweetened; participants likely can also distinguish CS and LNCS)]. Q5. Were the people assessing the outcomes blinded to the participants’ group assignments? Q6. Were the groups similar at baseline on important characteristics that could affect outcomes (e.g., demographics, risk factors, comorbid conditions)? Q7. Was the overall drop-out rate from the study at endpoint 20% or lower of the number allocated to treatment? Q8. Was the differential drop-out rate (between treatment groups) at endpoint 15 percentage points or lower? Q9. Was there high adherence to the intervention protocols for each treatment group? Q10. Were variables on the day of testing controlled (i.e., were participants requested to fast between breakfast and consumption of the preload and/or consume a standardized breakfast)? Q11. Were variables on the day before testing controlled (i.e., was an overnight fast required and were alcohol and/or physical activity restrictions similar in the groups)? Q12. Were outcomes assessed using valid and reliable measures, implemented consistently across all study participants? Q13. Did the authors report that the sample size was sufficiently large to be able to detect a difference in the main outcome between groups with at least 80% power? Q14. Were outcomes reported or subgroups analyzed prespecified (i.e., identified before analyses were conducted)? Q15. Were all randomized participants analyzed in the group to which they were originally assigned (i.e., did they use an intention-to-treat analysis)? CS, caloric sweetener; exp, experiment; LNCS, low-/no-calorie sweetener; NA, not applicable; NR, not reported; Q, question; UNS, unsweetened.

2Q10 was analyzed based on 2 criteria; a “yes” was required for each of the following: 1) participants were requested to fast and 2) participants consumed a standardized breakfast. If the publication did not account for both criteria, the publication received an “NR” for Q10. In the case where the breakfast was the preload or the ad libitum meal, question 10 is NA as the fasting period between the breakfast and preload could not be measured. In this circumstance, overnight fasting was mandatory the day prior to testing and was required in order to score question 11 as a “yes.”

3Q11 was analyzed based on 3 criteria; a “yes” was awarded if: i) participants were requested to fast overnight, AND EITHER 2) physical activity was standardized the night before each testing session OR 3) alcohol consumption was standardized the night before each testing session; otherwise, the publication received an “NR” for Q11.