Does a later morning session pay?
Two hours later gave adolescent swimmers 1 h more night sleep, 0.8 h counting naps, but no significant difference in time-trial change over 8 days. Both arms did the same doubles.
Thirty-four swimmers started; 27 finished both 8-day camps, in January and October 2023. Each camp had 13 sessions, six in the morning and seven in the afternoon, the same structure under the same head coach, with morning sessions at 07:00 or 09:00 and the order reversed at the second camp.
Night sleep rose from 5.9 ± 0.6 to 6.9 ± 0.8 h (mean difference 1.0 ± 0.5 h, p < 0.001), wake time moved from 05:36 to 07:18 and bedtime from 22:54 to 23:18. The early arm took more naps, so the 24-h gain narrowed to 0.8 ± 0.6 h. Sleep efficiency fell slightly in the late condition (81.0 to 79.6%, p = 0.03).
Time-trial changes showed no significant difference: 100 m interaction p = .629, 800 m p = .884. Across both conditions 800 m improved (p = .014), within the 8.7-s error the authors cite for hand timing. Emotional balance declined over the early camp only; other recovery scores showed no significant condition effect. Motivation before the tests was higher in the late condition.
Mediation showed no indirect path through sleep to mental capacity, nor through mental capacity to 100 m time. Our reading: a clean demonstration that training hour moves sleep, and a weak null on whether that hour moves performance in eight loaded days.
Protocol
Key Results
| Measure | Early (07:00) | Late (09:00) | Test |
|---|---|---|---|
| Night sleep (h) | 5.9 ± 0.6 | 6.9 ± 0.8 | difference 1.0 ± 0.5, p < 0.001 |
| 24-h sleep with naps (h) | 6.5 ± 0.6 | 7.3 ± 0.5 | difference 0.8 ± 0.6, p < .001 |
| Wake time | 05:36 ± 00:09 | 07:18 ± 00:25 | p < .001 |
| Bedtime | 22:54 ± 00:28 | 23:18 ± 00:32 | p < .001 |
| Number of naps | 2.3 ± 1.7 | 1.3 ± 1.1 | p = .023 |
| Sleep efficiency (%) | 81.0 ± 4.3 | 79.6 ± 4.4 | p = 0.03 |
| Perceived sleep quality | 3.3 ± 1.0 | 3.3 ± 0.7 | p = 0.50 |
| Daily session load (AU) | 1005 ± 258 | 964 ± 296 | p = .465 |
| 100 m (s), pre → post | 66.1 ± 5.4 → 65.9 ± 5.4 | 66.9 ± 5.5 → 67.0 ± 6.0 | interaction p = .629; condition p = .291 |
| 800 m (s), pre → post | 607.6 ± 37.2 → 600.2 ± 36.3 | 611.7 ± 37.7 → 605.2 ± 31.7 | interaction p = .884; time p = .014 |
| Motivation, pre → post | 56.8 ± 18.6 → 49.3 ± 22.1 | 64.1 ± 12.8 → 63.6 ± 20.1 | condition p = .011; interaction p = .259 |
| Mental capacity (0-6) | 3.2 ± 0.8 | 3.5 ± 0.9 | p = .084 |
| Emotional balance across days | b = −0.1, p = 0.001 | b = −0.0, p = 0.75 | condition × day p = 0.04 |
| Warm-up heart-rate change at 60% (bpm) | −1 ± 16 | −8 ± 13 | p = .080 |
Mechanisms
Practical Application
Limitations
How this entry was checked and changed
controlled crossover with n ≥ 15, read from the full text (CC BY). It sits at the low edge of the band: registration came more than two years after the camps (our arithmetic), performance analyses had 20-21 swimmers (our reading of the degrees of freedom), power was calculated only for sleep, and there was a period effect between camps