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Status

Completed

Conditions

Physical Activity
Obesity

Treatments

Behavioral: Affect and physical activity
Behavioral: Physical activity information

Study type

Interventional

Funder types

Other

Identifiers

NCT03598647
1179772

Details and patient eligibility

About

This study seeks to investigate why some individuals exercise more than others by focusing on feelings related to exercise. This two part study first examines whether regular exercisers (n=30) and non-exercisers (n=30) differ in how a 30-minute moderate-intensity exercise bout makes them feel. All participants will walk on a treadmill for 30 minutes on two separate occasions and will be asked to report on how they feel before, during, and after exercise, how they anticipate that exercise will make them feel, and how they remembered feeling during exercise. In addition, after exercise session #2, non-exercisers will be randomized to: 1) a brief intervention focused on providing general information about the physical activity guidelines, or 2) a brief intervention which provides general information about physical activity guidelines, but also focuses on affective responses to physical activity. Non-exercisers will complete an identical, third exercise session approximately 1-week following this intervention. Further, all participants will receive a 12-week, Internet-delivered weight loss program following all exercise visits and physical activity will be assessed before and after the weight loss program.

Enrollment

60 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-60 years
  • BMI between 25.0 and <40.0 kg/m2
  • Either a 'Non-exerciser', defined as reporting exercising at a moderate-intensity for <30 min/week over the past 6 months and a most recent typical week or an 'exerciser', defined as exercising for ≥150 min/week over the past 6 months and a most recent typical week.

Exclusion criteria

  • Presence of any condition that would limit one's ability to exercise (e.g., orthopedic limitations)
  • History of coronary artery disease (i.e., myocardial infarction or symptoms of angina), stroke, diabetes, or pulmonary disease (e.g., COPD or emphysema).
  • Currently taking any medication that would alter heart rate (e.g., beta blocker)
  • Women who are pregnant or nursing
  • Uncontrolled hypertension (resting blood pressure ≥140/90 mmHg)
  • Exercising >30 min/week but <150 min/week (i.e., neither 'non-exerciser' nor 'exerciser')
  • Use of medications for weight loss, or current participation in another weight loss program
  • Bariatric surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 4 patient groups

Physical activity information - for non-exercisers only
Active Comparator group
Description:
Non-exercisers randomized to this condition will receive basic information about physical activity. This includes the national physical activity guidelines,clarification of 'moderate-intensity', exercise safety, and the progression of physical activity within the weight loss program.
Treatment:
Behavioral: Physical activity information
Affect and physical activity - for non-exercisers only
Experimental group
Description:
Non-exercisers randomized to this condition will receive the same basic information about physical activity as described above, but they will also receive a brief intervention focused on affective responses to exercise.
Treatment:
Behavioral: Affect and physical activity
Exercisers
No Intervention group
Description:
Engaging in \>=150 min/week of moderate-intensity exercise over the past 6 months and a most recent typical week
Non-exercisers
No Intervention group
Description:
Engaging in \<30 min/week of moderate-intensity exercise over the past 6 months and a most recent typical week

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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