Hydration and Physical Activity
Recruitment not mentioned
Design
CES and placebo treatments during 4h recovery period, administered in double-blind, crossover design. Exercise trials (90 min treadmill running, or until fatigue, whichever reached first) in environmental chamber (35C, 40% RH).
Blinding used (if applicable): Double-blinded
Intervention (if applicable)
CES (commercially-available sports drink, 6.9%CHO, 24mmol 1-1 Na, 2.6 mmol 1-1 K, 1mmol 1-1 Cl) and placebo (flavored sweetened water) treatments during 4h recovery period
Statistical Analysis
Comparisons made after establishing normality (Anderson-Darling Goodness of Fit test).
Performance times, rate of change of tempertaure and HR were tested for treatment X run interaction, and data obtained over time tested for treat X time interaction(2-way ANOVA for repeated measures).
Sig interactions subjected to Tukey post-hoc analyses to identify differences between means.
Total volumes fluid consumed, Urine vol and body mass changes analyzed (Student's paired t-test);
Sig level at p<0.05.
Timing of Measurements
Pre-exercise: Standard breakfast; void bladder, body mass obtained; venous and capillary samples taken
T1: Treadmill running at 60% VO2 max for 90 min or until volitional fatigue; temp and HR recorded, along with expired gas every 60 sec. RPE and RPTD every 15 min.
Recovery: 3 equal feedings (equivalent to 100% weight loss) of treatment solution (CES or P) at 0, 1, 2 hr. after 3 h, void bladder, body mass recorded; bolus dose of treatment solution given to remaining fluid deficit (140% of body mass loss). Capillary samples taken every 60 min throughout recovery. Urine collected throughout recovery. Voided bladder at end of recovery.
T2: procedures from pre-exercise and T1 repeated; venous and capillary samples, body mass obtained at end of trial.
Dependent Variables
- Temp and HR (arual thermometer, ECG)
- VO2, VCO2, VE (expired gases -- infrared and dry gas meters) ---> calculate RER
- Body mass (scale)
- Hgb, packed cell vol, plasma vol
- Urine vol
- Rating of perceived exertion (RPE) and thermal discomfort (RPTD) (scales)
Independent Variables: CES or Placebo treatment during recovery period
Control Variables: temp and RH of environmental chamber (35C, 40%RH); standard breakfast before testing; running at 60% VO2max
Initial N: 13 trained M
Attrition (final N): 13
Age: 32.4±1.4 yr
Ethnicity: not mentioned
Other relevant demographics:
Anthropometrics: 178.2±1.4 cm; 79.4±2.8 kg; 16.5±1.0% body fat
Location: Laboratory, Institute Naval Medicine, Alverstoke, Gosport, Hampshire, UK
Variables |
T1 CES P |
Recovery CES P |
T2 CES P |
Statistical Significance of Group Difference |
Run times (min) |
74.8±4.6** 72.5±5.2** |
60.9±5.5* 44.9±3.0 |
*r=0.93, p<0.01, ces vs p *p<0.01 T1 vs T2 |
|
Pre-Exercise body mass (kg) |
78.82±2.88 78.42±2.90 |
|
|
|
Post-exercise body mass |
77.39±2.91 77.11±2.92 |
78.88±2.87 78.42±2.91 |
77.79±2.88 77.34±2.95 |
ns |
Fluid intake (g) |
757±50 728±50 |
2006±176 1830±165 |
615±57 452±35 |
ns |
Sweat loss (g) |
2167±156 2035±152 |
1705±187 1525±127 |
ns | |
Sweat rate (g/min) |
29.2±2.1 28.6±1.8 |
29.1±3.5 33.8±1.8* |
*p<0.05, p vs ces | |
Urine production (g) |
515±69 527±89 |
ns | ||
Net fluid balance (g) |
-1433±126 -1307±118 |
58±26 -4±68 |
-1032±170 -1077±148 |
ns |
Other Findings
Metabolic Measurements: progressive increase in VO2 over time during each exercise period, and in both conditions (p<0.01). Nature of E-metabolism did not differ between 2 treatments during T1, but RER values were higher at all time points during T2 of CES vs P (P<0.01).
Blood Measurements: plasma vol reduced after T1 and T2, compared to pre-exercise and recovery (respectively) in both conditions (p<0.01). No differences between CES and P in magnitude of calculated decrease in plasma vol. No differences in blood glucose between CES and P, or throughout T1. During recovery, blood glucose increased after 60 min (p<0.01), 120 min (p<0.01) and 180 min (p<0.05) of the CES vs P. Moderately severe hypoglycemic response seen after 30 min and at end of T2 during CES vs P (p<0.01). Blood lactate increased from resting after 30 min of exercise during both trials - no differences in magnitude of increase. No differences in blood lactate between CES and P at any time point during T2.
Thermal & Subjective Responses: NS treatment effects on Temp, HR, RPE, RPTD during T1. HR incr at end of T1 (P<0.01); Increases in Temp, RPE, RPTD (all p<0.01) during T1. HR and temp greater after 30 min exercise during T2 of P vs CES trial (P<0.05). Rate of HR increase per hour of exercise lower during T2 in CES vs P (P<0.01). RPE and RPTD higher after T2 during P vs CES (P<0.01 and p<0.05, respectively)
Ingesting a CES in sufficient quantities to replace body mass loss following prolonged, constant pace running in a warm environment improves endurance capacity 4 hours later.
6.9% CES facilitated rehydration as effectively as the flavored, sweetened water solution.
Provided that adequate hydration status is maintained, inclusion of CHO and electrolytes within a rehydration solution will delay onset of fatigue during subsequent bout of prolonged submaximal running in a warm environment.
Government: | Ministry of Defense (UK) |
Quality Criteria Checklist: Primary Research
|
|||
Relevance Questions | |||
1. | Would implementing the studied intervention or procedure (if found successful) result in improved outcomes for the patients/clients/population group? (Not Applicable for some epidemiological studies) | Yes | |
1. | Would implementing the studied intervention or procedure (if found successful) result in improved outcomes for the patients/clients/population group? (Not Applicable for some epidemiological studies) | Yes | |
2. | Did the authors study an outcome (dependent variable) or topic that the patients/clients/population group would care about? | Yes | |
2. | Did the authors study an outcome (dependent variable) or topic that the patients/clients/population group would care about? | Yes | |
3. | Is the focus of the intervention or procedure (independent variable) or topic of study a common issue of concern to dieteticspractice? | Yes | |
3. | Is the focus of the intervention or procedure (independent variable) or topic of study a common issue of concern to dieteticspractice? | Yes | |
4. | Is the intervention or procedure feasible? (NA for some epidemiological studies) | Yes | |
4. | Is the intervention or procedure feasible? (NA for some epidemiological studies) | Yes | |
Validity Questions | |||
1. | Was the research question clearly stated? | Yes | |
1. | Was the research question clearly stated? | Yes | |
1.1. | Was (were) the specific intervention(s) or procedure(s) [independent variable(s)] identified? | Yes | |
1.1. | Was (were) the specific intervention(s) or procedure(s) [independent variable(s)] identified? | Yes | |
1.2. | Was (were) the outcome(s) [dependent variable(s)] clearly indicated? | Yes | |
1.2. | Was (were) the outcome(s) [dependent variable(s)] clearly indicated? | Yes | |
1.3. | Were the target population and setting specified? | Yes | |
1.3. | Were the target population and setting specified? | Yes | |
2. | Was the selection of study subjects/patients free from bias? | Yes | |
2. | Was the selection of study subjects/patients free from bias? | Yes | |
2.1. | Were inclusion/exclusion criteria specified (e.g., risk, point in disease progression, diagnostic or prognosis criteria), and with sufficient detail and without omitting criteria critical to the study? | Yes | |
2.1. | Were inclusion/exclusion criteria specified (e.g., risk, point in disease progression, diagnostic or prognosis criteria), and with sufficient detail and without omitting criteria critical to the study? | Yes | |
2.2. | Were criteria applied equally to all study groups? | Yes | |
2.2. | Were criteria applied equally to all study groups? | Yes | |
2.3. | Were health, demographics, and other characteristics of subjects described? | Yes | |
2.3. | Were health, demographics, and other characteristics of subjects described? | Yes | |
2.4. | Were the subjects/patients a representative sample of the relevant population? | Yes | |
2.4. | Were the subjects/patients a representative sample of the relevant population? | Yes | |
3. | Were study groups comparable? | Yes | |
3. | Were study groups comparable? | Yes | |
3.1. | Was the method of assigning subjects/patients to groups described and unbiased? (Method of randomization identified if RCT) | Yes | |
3.1. | Was the method of assigning subjects/patients to groups described and unbiased? (Method of randomization identified if RCT) | Yes | |
3.2. | Were distribution of disease status, prognostic factors, and other factors (e.g., demographics) similar across study groups at baseline? | Yes | |
3.2. | Were distribution of disease status, prognostic factors, and other factors (e.g., demographics) similar across study groups at baseline? | Yes | |
3.3. | Were concurrent controls or comparisons used? (Concurrent preferred over historical control or comparison groups.) | Yes | |
3.3. | Were concurrent controls or comparisons used? (Concurrent preferred over historical control or comparison groups.) | Yes | |
3.4. | If cohort study or cross-sectional study, were groups comparable on important confounding factors and/or were preexisting differences accounted for by using appropriate adjustments in statistical analysis? | N/A | |
3.4. | If cohort study or cross-sectional study, were groups comparable on important confounding factors and/or were preexisting differences accounted for by using appropriate adjustments in statistical analysis? | N/A | |
3.5. | If case control study, were potential confounding factors comparable for cases and controls? (If case series or trial with subjects serving as own control, this criterion is not applicable.) | Yes | |
3.5. | If case control study, were potential confounding factors comparable for cases and controls? (If case series or trial with subjects serving as own control, this criterion is not applicable.) | Yes | |
3.6. | If diagnostic test, was there an independent blind comparison with an appropriate reference standard (e.g., "gold standard")? | N/A | |
3.6. | If diagnostic test, was there an independent blind comparison with an appropriate reference standard (e.g., "gold standard")? | N/A | |
4. | Was method of handling withdrawals described? | N/A | |
4. | Was method of handling withdrawals described? | N/A | |
4.1. | Were follow-up methods described and the same for all groups? | N/A | |
4.1. | Were follow-up methods described and the same for all groups? | N/A | |
4.2. | Was the number, characteristics of withdrawals (i.e., dropouts, lost to follow up, attrition rate) and/or response rate (cross-sectional studies) described for each group? (Follow up goal for a strong study is 80%.) | N/A | |
4.2. | Was the number, characteristics of withdrawals (i.e., dropouts, lost to follow up, attrition rate) and/or response rate (cross-sectional studies) described for each group? (Follow up goal for a strong study is 80%.) | N/A | |
4.3. | Were all enrolled subjects/patients (in the original sample) accounted for? | Yes | |
4.3. | Were all enrolled subjects/patients (in the original sample) accounted for? | Yes | |
4.4. | Were reasons for withdrawals similar across groups? | N/A | |
4.4. | Were reasons for withdrawals similar across groups? | N/A | |
4.5. | If diagnostic test, was decision to perform reference test not dependent on results of test under study? | Yes | |
4.5. | If diagnostic test, was decision to perform reference test not dependent on results of test under study? | Yes | |
5. | Was blinding used to prevent introduction of bias? | Yes | |
5. | Was blinding used to prevent introduction of bias? | Yes | |
5.1. | In intervention study, were subjects, clinicians/practitioners, and investigators blinded to treatment group, as appropriate? | Yes | |
5.1. | In intervention study, were subjects, clinicians/practitioners, and investigators blinded to treatment group, as appropriate? | Yes | |
5.2. | Were data collectors blinded for outcomes assessment? (If outcome is measured using an objective test, such as a lab value, this criterion is assumed to be met.) | Yes | |
5.2. | Were data collectors blinded for outcomes assessment? (If outcome is measured using an objective test, such as a lab value, this criterion is assumed to be met.) | Yes | |
5.3. | In cohort study or cross-sectional study, were measurements of outcomes and risk factors blinded? | Yes | |
5.3. | In cohort study or cross-sectional study, were measurements of outcomes and risk factors blinded? | Yes | |
5.4. | In case control study, was case definition explicit and case ascertainment not influenced by exposure status? | N/A | |
5.4. | In case control study, was case definition explicit and case ascertainment not influenced by exposure status? | N/A | |
5.5. | In diagnostic study, were test results blinded to patient history and other test results? | N/A | |
5.5. | In diagnostic study, were test results blinded to patient history and other test results? | N/A | |
6. | Were intervention/therapeutic regimens/exposure factor or procedure and any comparison(s) described in detail? Were interveningfactors described? | Yes | |
6. | Were intervention/therapeutic regimens/exposure factor or procedure and any comparison(s) described in detail? Were interveningfactors described? | Yes | |
6.1. | In RCT or other intervention trial, were protocols described for all regimens studied? | Yes | |
6.1. | In RCT or other intervention trial, were protocols described for all regimens studied? | Yes | |
6.2. | In observational study, were interventions, study settings, and clinicians/provider described? | N/A | |
6.2. | In observational study, were interventions, study settings, and clinicians/provider described? | N/A | |
6.3. | Was the intensity and duration of the intervention or exposure factor sufficient to produce a meaningful effect? | Yes | |
6.3. | Was the intensity and duration of the intervention or exposure factor sufficient to produce a meaningful effect? | Yes | |
6.4. | Was the amount of exposure and, if relevant, subject/patient compliance measured? | Yes | |
6.4. | Was the amount of exposure and, if relevant, subject/patient compliance measured? | Yes | |
6.5. | Were co-interventions (e.g., ancillary treatments, other therapies) described? | N/A | |
6.5. | Were co-interventions (e.g., ancillary treatments, other therapies) described? | N/A | |
6.6. | Were extra or unplanned treatments described? | N/A | |
6.6. | Were extra or unplanned treatments described? | N/A | |
6.7. | Was the information for 6.4, 6.5, and 6.6 assessed the same way for all groups? | Yes | |
6.7. | Was the information for 6.4, 6.5, and 6.6 assessed the same way for all groups? | Yes | |
6.8. | In diagnostic study, were details of test administration and replication sufficient? | Yes | |
6.8. | In diagnostic study, were details of test administration and replication sufficient? | Yes | |
7. | Were outcomes clearly defined and the measurements valid and reliable? | Yes | |
7. | Were outcomes clearly defined and the measurements valid and reliable? | Yes | |
7.1. | Were primary and secondary endpoints described and relevant to the question? | Yes | |
7.1. | Were primary and secondary endpoints described and relevant to the question? | Yes | |
7.2. | Were nutrition measures appropriate to question and outcomes of concern? | Yes | |
7.2. | Were nutrition measures appropriate to question and outcomes of concern? | Yes | |
7.3. | Was the period of follow-up long enough for important outcome(s) to occur? | Yes | |
7.3. | Was the period of follow-up long enough for important outcome(s) to occur? | Yes | |
7.4. | Were the observations and measurements based on standard, valid, and reliable data collection instruments/tests/procedures? | Yes | |
7.4. | Were the observations and measurements based on standard, valid, and reliable data collection instruments/tests/procedures? | Yes | |
7.5. | Was the measurement of effect at an appropriate level of precision? | Yes | |
7.5. | Was the measurement of effect at an appropriate level of precision? | Yes | |
7.6. | Were other factors accounted for (measured) that could affect outcomes? | Yes | |
7.6. | Were other factors accounted for (measured) that could affect outcomes? | Yes | |
7.7. | Were the measurements conducted consistently across groups? | Yes | |
7.7. | Were the measurements conducted consistently across groups? | Yes | |
8. | Was the statistical analysis appropriate for the study design and type of outcome indicators? | Yes | |
8. | Was the statistical analysis appropriate for the study design and type of outcome indicators? | Yes | |
8.1. | Were statistical analyses adequately described and the results reported appropriately? | Yes | |
8.1. | Were statistical analyses adequately described and the results reported appropriately? | Yes | |
8.2. | Were correct statistical tests used and assumptions of test not violated? | Yes | |
8.2. | Were correct statistical tests used and assumptions of test not violated? | Yes | |
8.3. | Were statistics reported with levels of significance and/or confidence intervals? | Yes | |
8.3. | Were statistics reported with levels of significance and/or confidence intervals? | Yes | |
8.4. | Was "intent to treat" analysis of outcomes done (and as appropriate, was there an analysis of outcomes for those maximally exposed or a dose-response analysis)? | N/A | |
8.4. | Was "intent to treat" analysis of outcomes done (and as appropriate, was there an analysis of outcomes for those maximally exposed or a dose-response analysis)? | N/A | |
8.5. | Were adequate adjustments made for effects of confounding factors that might have affected the outcomes (e.g., multivariate analyses)? | Yes | |
8.5. | Were adequate adjustments made for effects of confounding factors that might have affected the outcomes (e.g., multivariate analyses)? | Yes | |
8.6. | Was clinical significance as well as statistical significance reported? | N/A | |
8.6. | Was clinical significance as well as statistical significance reported? | N/A | |
8.7. | If negative findings, was a power calculation reported to address type 2 error? | N/A | |
8.7. | If negative findings, was a power calculation reported to address type 2 error? | N/A | |
9. | Are conclusions supported by results with biases and limitations taken into consideration? | Yes | |
9. | Are conclusions supported by results with biases and limitations taken into consideration? | Yes | |
9.1. | Is there a discussion of findings? | Yes | |
9.1. | Is there a discussion of findings? | Yes | |
9.2. | Are biases and study limitations identified and discussed? | Yes | |
9.2. | Are biases and study limitations identified and discussed? | Yes | |
10. | Is bias due to study's funding or sponsorship unlikely? | Yes | |
10. | Is bias due to study's funding or sponsorship unlikely? | Yes | |
10.1. | Were sources of funding and investigators' affiliations described? | Yes | |
10.1. | Were sources of funding and investigators' affiliations described? | Yes | |
10.2. | Was the study free from apparent conflict of interest? | Yes | |
10.2. | Was the study free from apparent conflict of interest? | Yes | |