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OpenTrials
Completed

NCT Number: NCT00143988

Heart Rate and Blood Pressure Response During Exercise and Sexual Activity in Normotensive and Hypertensive Volunteers

The purpose of this study is to determine the amount of cardiac work as measured by heart rate and blood pressure during physical exertion compared to sexual activity.

Completed

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Robert Wood Johnson University Hospital

New Brunswick, New Jersey, 08901, United States

About this study

Physical exertion will be measured by a standardized treadmill test. Sexual activity will be performed in the study subject's home with his/her spouse or regular partner. Each study subject will wear a blood pressure and heart rate monitor at home during their sexual activity and will be asked to complete a one page diary upon completion of the activity. Normotensive and subject with mild hypertension will be studied to determine if hypertensive subjects have a relatively greater increase in their blood pressure during either physical exercise or sexual activity.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion Criteri

  • Male or female age 40-80

Exclusion criteria

  • Current sexual partner less than six months duration or sexually inactive patients defined as engaging in sexual intercourse less than one time monthly
  • Uncontrolled hypertension (resting blood pressure >160/100); secondary hypertension; renal failure (serum creatinine >3.0); congestive heart failure (NYHA functional Class III-IV); acute coronary syndrome; PCI or open heart surgery within past 3 months; cerebrovascular disease within the past 6 months and any other major medical or psychiatric disorder.
  • Individuals who regularly (more than 3 times weekly) perform rigorous physical exercise.
  • Individuals unable to perform an exercise treadmill stress test.
  • Lack of informed consent

Treatment and study plan

Treadmill testing

Behavioral

Patients will have a exercise stress test using a Bruce protocol during which time heart rates and blood pressures will be monitored and the patient's percieved exertion level monitored and recorded

Other names: Quinton treadmill will be used

Ambulatory Blood Pressure and Heart Rate Monitoring

Behavioral

Patients will wear an ambulatory blood pressure monitor and an heart rate monitor during one sexual encounter.

Other names: Space Labs ambulatory BP monitor, Polar heart rate monitor

Primary outcomes

  1. physical stress during exercise

    Time frame: during one measured encounter

Sponsors and collaborators

Lead sponsor

University of Medicine and Dentistry of New Jersey

Other

Collaborators

  • Pfizer

Registry information

Acronym: SEXERRCISE

Important dates

Study start
2004
Primary completion
2007
Study completion
2007
First posted
Sep 2, 2005
Registry last updated
Aug 24, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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