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The Effect of Caffeine in Elderly Citizen Following Eight Hour Abstinence From Caffeine Containing Drinks & Foods

Phase 4
Completed
Conditions
Healthy
Elderly
Interventions
Registration Number
NCT01048515
Lead Sponsor
Herning Hospital
Brief Summary

The study investigated the effect of caffeine on physical performance in healthy citizens aged over 70 years following eight hours of abstinence from caffeine containing drinks and foods. The main hypothesis was that 6 mg/kg caffeine would improve cycling endurance at 65% of expected maximal heart rate.

Detailed Description

It is well documented that caffeine ingestion increases the endurance of young people exercising at 60%-85% of their maximal oxygen uptake (13;15;47). It also seems to improve endurance as measured by repeated sub-maximal isometric contraction (42), and decreases the rate of perceived exertion during exercise (6;9;46). Typically, doses of approximately 6 mg/kg caffeine were used in these studies.

With a growing number of elderly with a physical active lifestyle and many elderly participating in rehabilitation programs the endurance enhancing effect of caffeine is of increasing interest in this age group. We therefore conducted a study of healthy 75 year old citizens to investigate whether 6 mg/kg caffeine improved physical performance and reduced the perceived effort during work in healthy citizens aged ≥ 70 years. The main hypothesis was that caffeine would improve cycling endurance at 65% of expected maximal heart rate. The study showed that compared to placebo caffeine increased endurance by 25 % (p\<0.0001) and isometric sub-maximal strength with 54 % (p\<0.0001), reduced perceived exertion after 5 minutes of biking by 11 % (p=0.002), but in 21 of 30 participants there was reduced postural stability (with eyes open). In the above described study participants abstained from caffeine containing drinks and foods for 48 hours prior to each test. Half of the participants reported withdrawal symptoms. Such a long caffeine abstinence period would infer with daily life for many people. We therefore invited the participants from the above study to a repetition of the above study to test whether similar results would be obtained if participants only abstained from caffeine containing drinks and foods for 8 hours prior to each test.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Healthy elderly individuals aged over 70 years (Primarily those who previously have participated in an identical study with 48 hour caffeine abstinence)
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Exclusion Criteria
  • Dementia or invalidating psychiatric disease
  • General debility, angina, or other diseases that would render participation in the test program impossible
  • Treatment with beta receptor blocking drugs, calcium-channel blocking drugs, digitalis, or nitroglycerine
  • Acute disease and injury
  • Diabetes
  • Conditions that would contraindicate caffeine ingestion or participation in the test program
  • Treatment with medication that interacts with caffeine
  • Ingestion of caffeine containing drinks and foods 8 hours before each session
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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
CaffeineCaffeine-
PlaceboCaffeine-
Primary Outcome Measures
NameTimeMethod
Endurance measured on an ergometer bicycleThe tests started 1 h following placebo/caffeine
Secondary Outcome Measures
NameTimeMethod
Isometric endurance (arm flexion)The tests started 1 h following placebo/caffeine
Isometric maximum arm flexion strengthThe tests started 1 h following placebo/caffeine
Fatigue (Borg scale) during ergometer testAfter 5 minutes biking and at exhaustion
Postural stabilityThe tests started 1 h following placebo/caffeine
Reaction timeThe tests started 1 h following placebo/caffeine
Walking speedThe tests started 1 h following placebo/caffeine
Biochemistry: lactate, catecholamines, insulin, free fatty acids, glucoseBefore intervention; before cycling; after 5 minutes of cycling; and at exhaustion
Withdrawal symptomsAt the end of each test
Side effectsAt the end of each test

Trial Locations

Locations (1)

Surgical Research Department

🇩🇰

Herning, Midtjylland, Denmark

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