Althaus & Plunkett (2015) |
29 |
t(28) = 4.037, p < 0.001 |
0.76 |
0.98 |
0.38 |
16 |
57 |
Bahrick et al. (2013) |
16 |
t(15) = 5.26, p< .0001 |
1.32 |
0.99 |
0.66 |
7 |
21 |
Bahrick et al. (2015) |
16 |
t(15) = 3.27, p = .005 |
0.82 |
0.87 |
0.41 |
14 |
49 |
Baker, J.M., et al. (2014)* |
28 |
t(27) = 2.474, p = .02 |
0.49 |
0.70 |
0.24 |
35 |
139 |
Baker, R.K. et al. (2014) |
24 |
F(1, 88) = 6.56, p = .012 |
0.07 |
0.43 |
0.03 |
108 |
120 |
Bardi et al. (2014) |
12 |
t(11) = 2.768, p<.05 |
0.79 |
0.70 |
0.40 |
15 |
52 |
Benavides-Varela & Mehler (2015) |
22 |
t(21) = 2.123, p < .05 |
0.45 |
0.52 |
0.23 |
41 |
151 |
Bidet-Ildei et al. (2014) |
12 |
Z= 1.96; p<.05 |
1.37 |
0.99 |
0.69 |
|
|
Biro et al. (2014) |
12 |
t(22) = 2.54, p = .019 |
1.08 |
0.72 |
0.54 |
15 |
55 |
Bremner et al. (2013) |
12 |
F(1,10) = 10.95, p < .008 |
0.52 |
0.91 |
0.26 |
11 |
26 |
Brower & Wilcox (2013) |
10 |
t(18) = −0.58, p = .58 |
0.26 |
0.09 |
0.13 |
234 |
930 |
Cantrell et al. (2015) |
20 |
t(19) = 3.05 p = .007 |
0.68 |
0.82 |
0.34 |
19 |
70 |
Casasola & Park (2013) |
16 |
F(1, 15) = 5.38, p < .05 |
0.26 |
0.49 |
0.13 |
26 |
56 |
Cashon et al. (2013) |
23 |
t(22) = 3.44, p |
0.72 |
0.91 |
0.36 |
18 |
63 |
Coubart et al. (2014) |
16 |
F(1, 12) = 12.8, p = .004 |
0.52 |
0.97 |
0.26 |
11 |
26 |
Esteve-Gibert et al. (2015) |
24 |
F(1, 20) = 7.262, p = .014 |
0.27 |
0.31 |
0.13 |
25 |
56 |
Ferry et al. (2015) |
11 |
t(10) = 3.577, p = .005 |
1.07 |
0.89 |
0.54 |
9 |
24 |
Flom et al. (2014)* |
20 |
t(19) = 2.5, p = .02 |
0.56 |
0.66 |
0.28 |
28 |
103 |
Frick & Möhring (2013) |
20 |
F(1, 36) = 6.94, p < .05 |
0.16 |
0.27 |
0.08 |
14 |
26 |
Frick & Wang (2014)) |
7 |
t(13) = 2.82, p = .01 |
1.45 |
0.70 |
0.73 |
9 |
31 |
Gazes et al. (2015) |
32 |
F(1,28) = 10.21, p = .003 |
0.27 |
0.84 |
0.13 |
25 |
56 |
Graf Estes & Hay (2015)* |
16 |
t(15) = 2.28, p = .038 |
0.57 |
0.57 |
0.29 |
27 |
96 |
Gustafsson et al. (2015) |
30 |
F(1,29) = 4.588, p = 0.041 |
0.14 |
0.32 |
0.07 |
52 |
108 |
Henderson & Scott (2015)* |
16 |
t(15) = 2.20, p < 0.05 |
0.55 |
0.54 |
0.28 |
28 |
103 |
Hernik & Csibra (2015) |
16 |
t(15) = 2.65, p = .018 |
0.66 |
0.69 |
0.33 |
21 |
75 |
Heron-Delaney et al. (2013) |
18 |
t(17) = 2.44, p = .025 |
0.58 |
0.64 |
0.29 |
26 |
96 |
Hillairet de Boisferon et al. (2014) |
23 |
t(22) = 2.89, p < .01 |
0.60 |
0.78 |
0.30 |
24 |
90 |
Hillairet de Boisferon et al. (2015) |
18 |
t(17) = 2.29, p < .05 |
0.54 |
0.58 |
0.27 |
29 |
110 |
Hock et al. (2015) |
15 |
t(14) = 2.84, p<.02 |
0.73 |
0.75 |
0.37 |
17 |
60 |
Imura et al. (2015) |
19 |
t(18) = 4.39, p = 0.0004 |
1.01 |
0.98 |
0.51 |
10 |
33 |
Kampis et al. (2013) |
22 |
F(1,21) = 7.03, p= 0.015 |
0.25 |
0.61 |
0.13 |
27 |
56 |
Kavsek & Marks (2015) |
16 |
F(1, 15) = 55.13, p ≤ .001 |
0.79 |
1.00 |
0.39 |
5 |
16 |
Kwon et al. (2014) |
36 |
t(35) = 4.32, p < .001 |
0.72 |
0.99 |
0.36 |
18 |
63 |
Lee et al. (2015) |
23 |
t(21) = 2.60, p = 0.02 |
0.55 |
0.71 |
0.28 |
28 |
103 |
Lewkowicz (2013) |
35 |
F(1, 67) = 4.30, p < .05 |
0.06 |
0.09 |
0.03 |
126 |
257 |
Lewkowicz et al. (2015)* |
24 |
t(23) = 0.52, p = .30 |
0.11 |
0.08 |
0.06 |
651 |
2183 |
Libertus et al. (2014) |
16 |
t(15)= 2.7, p < .02 |
0.67 |
0.71 |
0.34 |
20 |
70 |
Liu et al. (2015)* |
11 |
t(10) = 3.16, p = |
0.95 |
0.81 |
0.48 |
11 |
37 |
Longh et al. (2015) |
15 |
F(1, 14) = 6.015, p < .028 |
0.30 |
0.58 |
0.15 |
22 |
48 |
Loucks & Sommerville (2013) |
13 |
t(12) = 2.38, p = .035 |
0.66 |
0.59 |
0.33 |
21 |
75 |
Mackenzie et al. (2014) |
16 |
t(15) = 3.56, p = .003 |
0.89 |
0.91 |
0.45 |
12 |
41 |
Matatyaho-Bullaro et al. (2014) |
12 |
t(11) = 6.44, p < .001 |
1.94 |
1.00 |
0.97 |
5 |
11 |
May & Werker (2014)* |
24 |
F(1, 22) = 10.67, p < .01 |
0.33 |
0.87 |
0.16 |
19 |
45 |
Moher & Feigenson (2013) |
18 |
F(1,16) = 21.996, p < .001 |
0.58 |
1.00 |
0.29 |
9 |
23 |
Novack et al. (2013)* |
16 |
t(15)=3.50, p<.003 |
0.88 |
0.91 |
0.44 |
13 |
43 |
Oakes & Kovack-Lesh (2013) |
12 |
t(11)=2.06, p=.06 |
0.59 |
0.46 |
0.30 |
25 |
90 |
Otsuka et al. (2013) |
12 |
t(11) = 3.04, p < .01 |
0.88 |
0.79 |
0.44 |
13 |
43 |
Ozturk et al. (2013) |
12 |
t(11) = 2.77, p < .02 |
0.80 |
0.71 |
0.40 |
15 |
52 |
Park & Casasola (2015) |
15 |
F(1, 32) = 20.86, p < .001 |
0.39 |
0.80 |
0.20 |
16 |
35 |
Perone & Spencer (2014)* |
39 |
t(38) = 3.50, p < .001 |
0.56 |
0.93 |
0.28 |
28 |
103 |
Pruden et al. (2013)* |
23 |
t(22) = 3.12, p < .05 |
0.65 |
0.84 |
0.33 |
21 |
75 |
Quinn & Liben (2014) |
12 |
t(11) = 5.14, p = |
1.48 |
0.99 |
0.74 |
6 |
17 |
Rigney & Wang (2013) |
18 |
F(1, 17)=10.83, p<.004 |
0.39 |
0.87 |
0.19 |
16 |
37 |
Robson et al. (2014)* |
24 |
t(23) = −2.305, p = .031 |
0.47 |
0.60 |
0.24 |
38 |
139 |
Sanefuji (2014) |
12 |
t(10) = 2.79, p = .019 |
0.84 |
0.75 |
0.42 |
14 |
47 |
Sato et al. (2013) |
14 |
t(13) = 3.04, p < 0.01 |
0.81 |
0.80 |
0.41 |
15 |
49 |
Skerry & Spelke (2014) |
32 |
F(1,31) = 8.524, p = 0.006 |
0.27 |
0.84 |
0.13 |
25 |
56 |
Slone & Johnson (2015) |
20 |
t(19) = 2.76, p < .05 |
0.62 |
0.75 |
0.31 |
23 |
84 |
Soley & Sebastián-Gallás (2015) |
32 |
t(31) = 2.42, p = .02 |
0.42 |
0.63 |
0.21 |
47 |
180 |
Starr et al. (2013) |
20 |
t(19) = 3.50, p < .005 |
0.78 |
0.91 |
0.39 |
15 |
54 |
Takashima et al. (2014) |
13 |
t(12) = 2.46, p < .05 |
0.68 |
0.62 |
0.34 |
19 |
70 |
Tham et al. (2015) |
12 |
t(10) = 2.342, p = .041 |
0.71 |
0.61 |
0.35 |
18 |
67 |
Träuble & Bätz (2014)* |
15 |
t(14) = ?4.09, p < .001 |
1.06 |
0.97 |
0.53 |
10 |
30 |
Tsuruhara et al. (2014) |
12 |
t(11) = 3.94, p < .01 |
1.14 |
0.95 |
0.57 |
9 |
27 |
Turati et al. (2013) |
17 |
F(1,14) = 5.489; p = 0.034 |
0.28 |
0.58 |
0.14 |
24 |
52 |
Vukatana et al. (2015) |
35 |
F(2, 68) = 3.27, p = .044 |
0.09 |
0.19 |
0.04 |
83 |
192 |
Woods & Wilcox (2013) |
15 |
F(1, 14)= 7.57, p =.02 |
0.35 |
0.71 |
0.18 |
18 |
39 |
Yamashita et al. (2014)* |
12 |
t(11) = 4.55, p = .0008 |
1.31 |
0.98 |
0.66 |
7 |
21 |
Zieber et al. (2014)* |
16 |
t(15) = 2.54, p = .02 |
0.64 |
0.67 |
0.32 |
22 |
79 |
Zieber et al. (2015) |
11 |
t(10) = 2.71, p < .03 |
0.81 |
0.63 |
0.41 |
15 |
49 |