Hydration and Physical Activity

Citation:
 
Study Design:
Class:
- Click here for explanation of classification scheme.
Quality Rating:
Research Purpose:
To assess whether ingesting carbohydrate-electrolyte solution (CES) during recovery from exercise in the heat (35C, 40%RH) influences endurance capacity 4 hours later. 
Inclusion Criteria:
Healthy, informed/written consent; no others mentioned
Exclusion Criteria:
None mentioned
Description of Study Protocol:

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.

Data Collection Summary:

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

 

Description of Actual Data Sample:

 

Initial N: 13 trained M

Attrition (final N): 13

Age32.4±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

 

Summary of Results:

 

 

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)

Author Conclusion:

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.

Funding Source:
Government: Ministry of Defense (UK)
Reviewer Comments:
Including CHO and electrolytes within rehydration/recovery period after exercise will delay onset of fatigue during a subsequent bout of prolonged activity. 
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