Exercise Counseling

-------------------------------------------------------------------------------

 
Recommendation
 
Clinicians should counsel all patients to engage in a 
program of regular physical activity, tailored to their 
health status and personal lifestyle.
 
Burden of Suffering
 
Physical inactivity has been associated with a number of 
debilitating medical conditions in the United States, 
including coronary artery disease (CAD), hypertension, 
noninsulin-dependent diabetes mellitus (NIDDM), and 
osteoporosis.  CAD is the leading cause of death in the 
United States, accounting for about 1.5 million myocardial 
infarctions and over 520,000 deaths each year.1,2  About 
400,000 Americans are victims of sudden death each year, 
due primarily to underlying atherosclerotic disease.  
Hypertension, which occurs in up to 58 million Americans,3 
is a leading risk factor for CAD, as well as for other 
serious diseases such as renal disease, retinopathy, and 
stroke.  Cerebrovascular disease alone accounts for about 
150,000 deaths each year and is the third leading cause of 
death in the United States.1  NIDDM is an important risk 
factor for CAD, cerebrovascular disease, retinopathy, and 
hypertension.  Nearly 6 million Americans suffer from 
NIDDM.4  Osteoporosis is responsible for an estimated 1.3 
million fractures each year.5  About one-quarter of all 
women over age 60 have spinal compression fractures, and 
about 15% of women sustain hip fractures during their 
lifetime.6,7  There is a 15-20% reduction in expected 
survival in the first year following a hip fracture.8  Hip 
fractures cost the United States over $7 billion each year 
in direct and indirect costs.9  

Efficacy of Risk Reduction
 
Studies have shown that men who are physically active on a 
regular basis have a lower overall mortality than those who 
are physically inactive.10,11  Exercise appears to be 
especially effective in improving health status in six 
disease-specific areas:  CAD, hypertension, obesity, NIDDM, 
osteoporosis, and diminished psychological well-being.
 
Physically inactive persons are twice as likely to develop 
CAD as are persons who engage in regular physical 
activity.12  Evidence from cohort studies has shown a 
consistent association between physical activity and 
reduced incidence of CAD.11,13,14  Similar benefits from 
exercise have been reported in older men (up to age 
75);15,16 efficacy in women is presumed on the basis of 
extrapolation.  Studies have also shown that exercise may 
have a beneficial effect on plasma lipoprotein 
concentrations.17  A possible criticism of the apparent 
benefits of exercise is that those who are physically 
active are at decreased risk for CAD by virtue of 
self-selection--that is, persons who choose to exercise may 
be inherently more healthy and have fewer overall risk 
factors for CAD.  However, studies controlling for such 
confounding variables have found that the effects of 
exercise are independent of other CAD risk factors, and 
that the cardiovascular benefits may even be augmented in 
the presence of other risk factors for CAD.16,18  It has 
also been shown that the type of individual who adopts 
athletic behavior is not protected from CAD if regular 
exercise is discontinued.  A study of former college 
athletes who had become physically inactive found that CAD 
risk in this cohort was similar to that of inactive alumni 
who had not been college athletes.19
 
Regular exercise is an important means of improving caloric 
balance and preventing obesity.  A large body of 
epidemiologic evidence supports an association between 
physical activity and weight control, even after 
controlling for dietary factors.20  The contribution of 
physical activity to daily caloric expenditure is often 
relatively small.  For example, a daily one-mile walk may 
amount to only a 4% contribution to total daily 
expenditure.  However, weight gain often occurs as a result 
of small differences between caloric intake and 
expenditures, and therefore it is possible through regular 
exercise to achieve a caloric balance that prevents 
progressive increases in weight.  Although exercise may 
increase caloric intake, it is accompanied by an even 
greater increase in caloric expenditure, so that a negative 
caloric balance is maintained.21
 
Exercise may reduce the risk of developing hypertension and 
NIDDM.  Cohort studies suggest that physically inactive 
persons have a 35-52% greater risk of developing 
hypertension than those who exercise; this effect appears 
to be independent of other risk factors for 
hypertension.22,23  The average reduction in blood pressure 
achieved through regular exercise has been estimated to be 
about 10 mm Hg.24  Physical activity is also associated 
with increased insulin sensitivity and glucose clearance, 
and epidemiologic studies of South Pacific natives suggest 
that differences in physical activity may have contributed 
to the increased prevalence of NIDDM in this 
population.25,26  Further evidence is needed, however, to 
prove that exercise improves glucose tolerance or that it 
reduces the risk of developing NIDDM.27
 
Weight-bearing physical activity may also reduce bone loss 
in postmenopausal women.28-34  Further research is needed 
to prove that bone mineral content is improved sufficiently 
to reduce the incidence of osteoporosis-related fractures.  
Although studies suggest the risk of hip fractures is lower 
in persons who exercise regularly,35,36 prospective 
evidence is necessary to prove that this effect is due 
specifically to exercise.  Additional studies are also 
needed to determine whether the risk of fall-related 
fractures during exercise offsets the intended benefits of 
preventing osteoporosis.
 
A commonly mentioned benefit of regular exercise is 
improved affect (positive mood, reduced depression, lowered 
anxiety).37,38  The nature of the relationship between 
exercise and mental health is poorly understood.  It is 
known that physically active persons report higher levels 
of self-esteem, perhaps in response to improved personal 
appearance and self-image.  No well-designed studies have 
shown that the incidence of clinically confirmed 
psychiatric disorders can be reduced through exercise.39  

Most studies have used different definitions for physical 
activity,40 and therefore it is not clear from the evidence 
exactly what form of exercise is most beneficial.  To 
improve cardiovascular fitness, it is known that exercise 
cannot be performed occasionally or seasonally,41 nor can 
one expect protection from CAD by having exercised 
regularly in the past.19  The cardiovascular effects at 
increasing levels of exercise intensity appear to operate 
in a dose-response relationship, with modest benefits at 
low energy expenditures (150-500 kcal/week) and maximal 
benefits at higher levels (2000-3500 kcal/week).10,19  
Small increases in activity among the most inactive persons 
appear to be associated with the largest magnitudes of risk 
reduction.  It has traditionally been thought that an 
improvement in cardiovascular fitness requires a threshold 
level of aerobic intensity during an exercise session and a 
minimum frequency of sessions, and this has served as the 
basis for a number of similar exercise criteria.  Three of 
these include:  (1) dynamic movement of large muscle groups 
for at least 20 minutes, three or more days per week, 
performed at an intensity of at least 60% of 
cardiorespiratory capacity; (2) intensity of 50-100% of 
cardiorespiratory capacity, frequency of two to four times 
per week, duration of 15-45 minutes, program length of 5-11 
weeks; and (3) achieving and maintaining a pulse rate equal 
to the formula: (220 - age) x 70%.42,43
 
It has also become clear that many of the health benefits 
of exercise may be obtained even at lower intensity and 
frequency levels.  Furthermore, vigorous exercise may not 
be advisable in some individuals, especially those who are 
at increased risk of injury or cardiovascular complications 
from vigorous physical activity (e.g., the elderly).  A 
number of studies suggest that the threshold intensity for 
improving cardiovascular fitness may be lower than 
previously thought and that activities such as brisk 
walking, climbing stairs, and gardening can be 
beneficial.11,18,40,41,44  These benefits have been 
validated in studies of low intensity activity in elderly 
persons44-47 and those with poor baseline fitness.43  
Inactive persons, as well as those who are hypertensive or 
obese, can benefit significantly from even modest increases 
in physical activity.  In addition, as described above, 
persons who engage in low intensity exercise may also enjoy 
the benefits of exercise other than those relating to CAD; 
these include improved strength and flexibility (which may 
reduce the risk of falls in the elderly; see Chapter 52), 
increased bone density, and improved mood.  

The benefits of exercise must be weighed against its 
potential adverse effects, which include injury, 
osteoarthritis, and, rarely, sudden death.  Although 
injuries are commonly reported in competitive sports, there 
are few reliable data on the incidence of injuries during 
typical noncontact exercises.48,49  It is currently thought 
that most injuries during exercise are preventable.  They 
often occur as a result of excessive levels of physical 
activity, dramatic incremental changes in activity level 
(especially in persons with poor baseline fitness), and 
improper exercise techniques or equipment.  A second 
concern is that long-term physical activity may accelerate 
the development of osteoarthritis in major weight-bearing 
joints (e.g., hips, knees).  Cross-sectional studies in 
long-distance runners, however, have been unable to 
demonstrate a strong association between exercise and 
osteoarthritis.50-52  A third concern is the risk of sudden 
death, which is known to be increased during vigorous 
physical activity.53  Studies suggest that sedentary 
persons who engage in vigorous activity are at greater risk 
for sudden death than are those who are regularly active.54 
 In fact, due to the cardiovascular benefits of exercise, 
the overall risk of sudden death (both during and not 
during exercise) in men who engage regularly in high levels 
of physical activity is considerably lower than in 
sedentary men.54  

Effectiveness of Counseling
 
At least 40% of the U.S. population is considered 
sedentary, and as many as 80-94% fail to exercise at an 
adequate level to obtain cardiorespiratory benefit.55,56  
Thus, the majority of patients seen by physicians could 
potentially benefit from encouragement to increase physical 
activity levels.  There is, however, a limited amount of 
information regarding the ability of physicians to 
influence the exercise behavior of patients.  Studies that 
have demonstrated benefits from counseling provide little 
information about long-term compliance and are of limited 
generalizability, because the form of counseling, type of 
patients, or clinical setting have not been representative 
of typical primary care physician counseling of healthy 
patients.57-63  It is known from surveys, however, that 
negative perceptions of exercise activity (e.g., 
inconvenience, cost of equipment, discomfort) can often act 
as powerful disincentives.64,65  In particular, 
high-intensity activities and greater perceived exertion 
are major barriers to adherence to physical activity 
programs, especially in sedentary persons over the age of 
35.  Persons most likely to adopt vigorous exercise 
programs are those already exercising at a moderate 
level.65
 
Recommendations of Others
 
Although counseling patients to exercise is widely 
recognized as clinically prudent, there are few official 
recommendations for physicians to include exercise 
counseling in the periodic health examination.  The 
American College of Sports Medicine has issued specific 
guidelines on the medical contraindications to exercise.66
 
Discussion
 
Despite the absence of direct evidence that physician 
counseling can increase the physical activity of 
asymptomatic patients, the intervention is warranted 
because of the numerous potential health benefits 
associated with physical activity.  Physical inactivity 
results in a slightly lower relative risk for CAD than the 
commonly accepted risk factors of hypertension, 
hypercholesterolemia, and cigarette smoking, but it is a 
much more common cardiac risk factor in the U.S. 
population.67  Physical inactivity is also a risk factor 
for other serious diseases, such as hypertension and 
obesity.  Thus, from a population perspective, even modest 
increases in physical activity levels could have large 
public health implications.67
 
Nonetheless, it is important for clinicians to use 
discretion in recommending appropriate forms of physical 
activity for patients.  In addition to considering 
potential contraindications in persons with underlying 
medical disorders, it is also necessary to design an 
exercise program with an awareness of potential barriers to 
compliance in the patient's personal lifestyle.  Since some 
patients will be unable or unwilling to engage in any high 
intensity activities, recommending low intensity exercise 
for certain individuals may ultimately achieve greater 
health benefits than urging vigorous exercise activities.  
Brisk walking, for example, offers improved cardiovascular 
fitness along with the compliance-enhancing features of 
convenience, lower perceived discomfort, and safety.  The 
addition of a strong arm swing (aerobic or "pace" walking), 
although slightly more difficult technically, is a simple 
measure to increase the aerobic activity of walking.
 
Clinical Intervention
 
Clinicians should provide all patients with information on 
the role of physical activity in disease prevention and 
assist in selecting an appropriate type of exercise.  
Factors that should be considered in designing a program 
include medical limitations and activity characteristics 
that both improve health (e.g., weight-bearing, increased 
caloric expenditure, enhanced cardiovascular fitness, low 
potential adverse effects) and enhance compliance (e.g., 
low perceived exertion, cost, inconvenience).  The patient 
should also be given instructions on how to perform the 
exercise safely to reduce the risk of injuries.  The 
patient should be encouraged to set at least one specific 
exercise goal; the initial target should be only a small 
increment above baseline status.  Beginners should 
emphasize regular, rather than vigorous, exercise; an 
appropriate short-term goal is to engage in regular walking 
at least three times per week for at least 30 minutes.  
Ultimately, over a period of several months, the patient 
should progress to a level that achieves increased 
cardiovascular fitness (e.g., 30 minutes of daily brisk 
walking).  For most healthy persons, maximum cardiovascular 
fitness can be achieved by a program of vigorous aerobic 
exercise for 15-45 minutes, two to four times per week, 
during which a pulse rate of about (220 - age) x 70% is 
reached and maintained.  Clinicians who are unable to 
design an effective exercise program may wish to refer 
patients to an accredited fitness center or exercise 
specialist.
 
Note:  See Appendix A for the U.S. Preventive Services Task 
Force Table of Ratings for this topic.  See also the 
relevant Task Force background paper:  Harris SS, Caspersen 
CJ, DeFriese GH, et al. Physical activity counseling for 
healthy adults as a primary preventive intervention in the 
clinical setting; report for the U.S. Preventive Services 
Task Force. JAMA 1989;261:3590-8.
 
References
 
1. National Center for Health Statistics.  Advance report 
of final mortality statistics, 1986.  Monthly Vital 
Statistics Report [Suppl], vol. 37, no. 6.  Hyattsville, 
Md.: Public Health Service, 1988.  (Publication no. DHHS 
(PHS) 88-1120.)
 
2. American Heart Association.  1989 heart facts.  Dallas, 
Tex.: American Heart Association, 1988.
 
3. 1988 Joint National Committee.  The 1988 report of the 
Joint National Committee on Detection, Evaluation, and 
Treatment of High Blood Pressure.  Arch Intern Med 1988; 
148:1023-38.
 
4. National Center for Health Statistics.  Current 
estimates from the National Health Interview Survey, United 
States, 1982.  Vital and Health Statistics, series 10, no. 
150.  Washington, D.C.: Government Printing Office, 1985.  
(Publication no. DHHS (PHS) 85-1578.)
 
5. Consensus conference statement: osteoporosis.  JAMA 
1984; 252:799-802.
 
6. Melton LJ III.  Epidemiology of fractures.  In: Riggs 
BL,  Melton LJ III.  Osteoporosis: etiology, diagnosis, and 
management.  New York: Raven Press, 1988.
 
7. Cummings SR, Kelsey JL, Nevitt MC, et al.  Epidemiology 
of osteoporosis and osteoporotic fractures. Epidemiol Rev 
1985; 7:178-208.
  8. Jensen GF, Christiansen C, Boesen J, et al.  
Epidemiology of postmenopausal spinal and long bone 
fractures: a unifying approach to postmenopausal 
osteoporosis.  Clin Orthoped 1982; 166:75-81.
 
9. Holbrook TL, Grazier K, Kelsey JL, et al.  The frequency 
of occurrence, impact, and cost of selected musculoskeletal 
conditions in the United States.  Chicago, Ill.: American 
Academy of Orthopedic Surgeons, 1984.
 
10. Paffenbarger RS Jr, Hyde RT, Wing AL, et al.  Physical 
activity, all-cause mortality, and longevity of college 
alumni.  N Engl J Med 1986; 314:605-13.
 
11. Leon AS, Connett J, Jacobs DR, et al.  Leisure-time 
physical activity levels and risk of coronary heart disease 
and death.  The Multiple Risk Factor Intervention Trial.  
JAMA 1987; 258:2388-95.
 
12. Powell KE, Thompson PD, Caspersen CJ, et al.  Physical 
activity and the incidence of coronary heart disease.  Ann 
Rev Public Health 1987; 8:253-87.
 
13. Kannel WB, Wilson P, Blair SN.  Epidemiological 
assessment of the role of physical activity and fitness in 
the development of cardiovascular disease.  Am Heart J 
1985; 109:876-85.
 
14. Donahue RP, Abbott RD, Reed DM, et al.  Physical 
activity and coronary heart disease in middle-aged and 
elderly men: the Honolulu Heart Program.  Am J Public 
Health 1988; 78:683-5.
 
15. Morris JN, Pollard R, Everitt MG, et al.  Vigorous 
exercise in leisure-time: protection against coronary 
events.  Lancet 1980; 8206:1207-10.
 
16. Siscovick DS, Weiss NS, Fletcher RH, et al.  Habitual 
vigorous exercise and primary cardiac arrest: effect of 
other risk factors on the relationship.  J Chronic Dis 
1984; 37:625-31.
 
17. Wood PD, Haskell WL, Blair SN, et al.  Increased 
exercise level and plasma lipoprotein concentrations: a 
one-year, randomized, controlled study in sedentary, 
middle-aged men.  Metabolism 1983; 32:31-9.
 
18. Paffenbarger RS Jr, Wing AL, Hyde RT.  Physical 
activity as an index of heart risk in college alumni. Am J 
Epidemiol 1978; 108:161-75.
 
19. Paffenbarger RS Jr, Hyde RT, Wing AL, et al.  A natural 
history of athleticism and cardiovascular health. JAMA 
1984; 252:491-5.
 
20. Epstein LH, Wing RR.  Aerobic exercise and weight.  
Addict Behav 1980; 5:371-8.
 
21. Wood PD, Terry RB, Haskell WL.  Metabolism of 
substrates: diet, lipoprotein metabolism, and exercise. 
Federation Proc 1985; 44: 358-63.
 
22. Paffenbarger RS Jr, Wing AL, Hyde RT, et al.  Physical 
activity and the incidence of hypertension in college 
alumni.  Am J Epidemiol 1983; 117:245-6.
 
23. Blair SN, Goodyear NN, Gibbons LW, et al.  Physical 
fitness and incidence of hypertension in healthy 
normotensive men and women.  JAMA 1984; 252:487-90. 24. 
Bouchard C, Shephard RJ, Stephens T, et al., eds.  
Exercise, fitness, and health: research and consensus. 
Proceedings of the International Conference on Exercise, 
Fitness, and Health.  Champaign, Ill.: Human Kinetics 
Publishers (in press).
 
25. King H, Taylor R, Zimmet P, et al.  
Non-insulin-dependent diabetes in a newly independent 
Pacific nation: the Republic of Kiribati.  Diabetes Care 
1984; 7:409-15.
 
26. Zimmet P, Faaiuso S, Ainuu J, et al.  The prevalence of 
diabetes in the rural and urban Polynesian population of 
Western Samoa.  Diabetes 1981; 30:45-51.
 
27. Rauramaa R.  Relationship of physical activity, glucose 
tolerance and weight management.  Prev Med 1984; 13:37-46.
 
28. Mazess RB, Wheedon GD.  Immobilization and bone.  
Calcif Tissue Int 1983; 35:265-7.
 
29. Nilsson BE, Westlin NE.  Bone density in athletes.  
Clin Orthop 1971; 77:179-82.
 
30. Dalen N, Olsson KE.  Bone mineral content and physical 
activity.  Acta Orthop Scand 1974; 45:170-4.
 
31. Smith EL, Reddan W, Smith PE.  Physical activity and 
calcium modalities for bone mineral increase in aged women. 
 Med Sci Sports Exerc 1981; 13:60-4.
 
32. Smith EL, Reddan W.  Physical activity: a modality for 
bone accretion in the aged.  Am J Roentgenol 1976; 
126:1297.
 
33. Aloia JF, Conn SH, Ostani JA, et al.  Prevention of 
involutional bone loss by exercise.  Ann Intern Med 1978; 
89:356-8.
 
34. Krolner B, Toft B, Nielson SP, et al.  Physical 
exercise as prophylaxis against involutional vertebral bone 
loss: a controlled clinical trial.  Clin Sci 1983; 541-6.
 
35. Paganini-Hill A, Ross RK, Gerkins JR, et al.  
Menopausal estrogen therapy and hip fractures.  Ann Intern 
Med 1981; 95:28-31.
 
36. Chalmers J, Ho KC.  Geographic variations in senile 
osteoporosis: the association of physical activity.  J Bone 
Joint Surg 1970; 52:667-75.
 
37. Stephens T.  Physical activity and mental health in the 
United States and Canada: evidence from four population 
surveys.  Prev Med 1988; 17:35-47. 

38. Folkins CH, Sime WE.  Physical fitness training and 
mental health.  Am Psychol 1981; 36:373-89.
 
39. Hughes JR.  Psychological effects of habitual aerobic 
exercise: a critical review.  Prev Med 1984; 13:66-78.
  40. LaPorte RE, Adams LL, Savage DD, et al.  The spectrum 
of physical activity, cardiovascular disease and health: an 
epidemiologic perspective.  Am J Epidemiol 1984; 
120:507-17.
 
41. Magnus K, Matroos A, Strackee J.  Walking, cycling, 
gardening with or without seasonal interruption in relation 
to acute coronary events.  Am J Epidemiol 1979; 
110:724-33.
 
42. American College of Sports Medicine.  Position 
statement on the recommended quantity and quality of 
exercise for developing and maintaining fitness in healthy 
adults.  Med Sci Sports Exerc 1978; 10:7-10.
 
43. Wenger HA, Bell GJ.  The interactions of intensity, 
frequency and duration of exercise training in altering 
cardiorespiratory fitness.  Sports Med 1986; 3:346-56.
 
44. Haskell WL, Montoye HJ, Orenstein D.  Physical activity 
and exercise to achieve health-related physical fitness 
components.  Public Health Rep 1985; 100:202-12.
 
45. Badenhop DT, Cleary P, Schaal SF, et al.  Physiologic 
adjustments to higher- or lower-intensity exercise in 
elders.  Med Sci Sports Exerc 1983; 15:496-502.
 
46. DeVries HA.  Exercise intensity threshold for 
improvement of cardiovascular-respiratory function in older 
men.  Geriatrics 1971; 26:94-101.
 
47. Emes CG.  The effects of a regular program of light 
exercise on seniors.  J Sports Med Phys Fitness 1979; 
19:185-9.
 
48. Kraus JF, Conroy C.  Mortality and morbidity from 
injuries in sports and recreation.  Ann Rev Public Health 
1984; 5:163-92.
 
49. Koplan JP, Siscovick DS, Goldbaum GM.  The risks of 
exercise: a public health view of injuries and hazards.  
Public Health Rep 1985; 101:189-94.
 
50. Sohn RS, Michel LJ.  The effects of running on the 
pathogenesis of osteoarthritis of the hips and knees. Clin 
Orthop Rel Res 1985; 198:106-9. 

51. Panish RS, Schmidt C, Caldwell JR, et al.  Is running 
associated with degenerative joint disease?  JAMA 1986; 
255:1152-4.
 
52. Lane NE, Bioch DA, Jones HH, et al.  Long distance 
running, bone density and osteoarthritis.  JAMA 1986; 
255:1147-51.
 
53. Thompson PD, Fink EJ, Carleton RA, et al.  Incidence of 
death through jogging in Rhode Island from 1975 through 
1980.  JAMA 1982; 247:2535-8.
 
54. Siscovick DS, Weiss NS, Fletcher RH, et al.  The 
incidence of primary cardiac arrest during vigorous 
exercise.  N Engl J Med 1984; 311:874-7.
 
55. Caspersen CJ, Christenson GM, Pollard RA.  Status of 
the 1990 physical fitness objectives: evidence from NHIS 
1985.  Public Health Rep 1986; 101:587-92. 56. Stephens T, 
Jacobs DR Jr, White CC.  A descriptive epidemiology of 
leisure time physical activity.  Public Health Rep 1985; 
100:147-58.
 
57. Mulder JA.  Prescription home exercise therapy for 
cardiovascular fitness.  J Fam Pract 1981; 13:345-8.
 
58. Campbell MJ, Browne D, Waters WE.  Can general 
practitioners influence exercise habits? Controlled trial. 
Br Med J 1985; 290:1044-6. 

59. Dishman RK.  Compliance/adherence in health-related 
exercise.  Health Psychol 1982; 1:237-67.
 
60. Blair SN.  Physical activity leads to fitness and pays 
off.  Physician Sports Med 1985; 13:153-7.
 
61. Kriska AM, Bayles JA, Cauley RE, et al.  A randomized 
exercise trial in older women: increased activity over two 
years and the factors associated with compliance.  Med Sci 
Sports Exerc 1986; 18:557-62.
 
62. Iverson DC, Fielding JE, Crow RS, et al.  The promotion 
of physical activity in the United States population: the 
status of programs in medical, worksite community, and 
school settings.  Public Health Rep 1985; 100:212-24. 

63. Blair SN, Piserchia PV, Wilbur CS, et al.  A public 
health intervention model for work-site health promotion.  
JAMA 1986; 255:921-6.
 
64. Dishman RK, Sallis JF, Orenstein DR.  The determinants 
of physical activity and exercise.  Public Health Rep 1985; 
100:158-71.
 
65. Sallis JF, Haskell WL, Fortmann SP, et al.  Predictors 
of adoption and maintenance of physical activity in a 
community sample.  Prev Med 1986; 15:331-41.
 
66. American College of Sports Medicine.  Guidelines for 
graded exercise testing and exercise prescription. 
Philadelphia: Lea and Febiger, 1975. 

67. Centers for Disease Control.  Protective effect of 
physical activity on coronary heart disease.  MMWR 1987; 
36:426-30.
 
.