NCT02560792

Brief Summary

The primary goal of this study is to determine experimentally the relationship between affective response to exercise and future exercise behavior. A secondary goal is to examine potential mediators and moderators of this relationship, specifically four variables considered to contribute to the volitional control of exercise behavior - planning, attention, resource commitment, and affect regulation. An additional goal is to examine how symptoms of depression might influence the affective response to exercise, and the relationship between affective response to exercise and exercise behavior.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
101

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2009

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2009

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2010

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2010

Completed
5.5 years until next milestone

First Submitted

Initial submission to the registry

July 30, 2015

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 25, 2015

Completed
Last Updated

September 25, 2015

Status Verified

September 1, 2015

Enrollment Period

4 months

First QC Date

July 30, 2015

Last Update Submit

September 24, 2015

Conditions

Outcome Measures

Primary Outcomes (2)

  • Days of exercise according to prescription as measured by exercise log

    Number of days of prescribed exercise recorded on exercise log

    7 days

  • Days of exercise according to prescription as measured by heart rate monitor

    Number of days of prescribed exercise recorded by heart rate monitor

    7 days

Secondary Outcomes (3)

  • Intentions to exercise according to prescription as measured by intention to exercise scale

    5 minutes post-intervention

  • Volitional control of exercise: Planning as measured by exercise planning scale

    7 days post-intervention

  • Volitional control of exercise: Commitment as measured by commitment to exercise scale

    7 days post-intervention

Other Outcomes (4)

  • Positive activated affect as measured by Physical Activity Affect Scale

    5 minutes before, 10 and 20 minutes during, and 5 minutes after intervention

  • Negative activated affect as measured by Physical Activity Affect Scale

    5 minutes before, 10 and 20 minutes during, and 5 minutes after intervention

  • Tranquility as measured by Physical Activity Affect Scale

    5 minutes before, 10 and 20 minutes during, and 5 minutes after intervention

  • +1 more other outcomes

Study Arms (3)

Positive Affect Condition

EXPERIMENTAL

Participants read that their exercise prescription was a healthy level of intensity for exercise, and then read that most people indicated this level of intensity leads to positive affect. To further encourage participants to think about how the supposed typical affective response might apply to them personally, they were also asked to describe how they thought the exercise might lead to positive feelings.

Behavioral: Positive Affect Condition

Negative Affect Condition

EXPERIMENTAL

Participants read that their exercise prescription was a healthy level of intensity for exercise, and then read that most people indicated this level of intensity leads to negative affect. To further encourage participants to think about how the supposed typical affective response might apply to them personally, they were also asked to describe how they thought the exercise might lead to negative feelings.

Behavioral: Negative Affect Condition

Control Condition

EXPERIMENTAL

Participants read that their exercise prescription was a healthy level of intensity for exercise - affect was not mentioned.

Behavioral: Control Condition

Interventions

Participants read: "Most people exercising at this intensity say that it feels good, and that it makes them feel energized and more positive, and more relaxed afterwards. Thinking about your exercise prescription, please list the reasons or ways in which you, personally, might expect this exercise to lead to positive feelings, and what specifically about this exercise might make you, personally, feel good."

Positive Affect Condition

Participants read: "Most people exercising at this intensity say that it doesn't feel very good, and that it makes them feel tired and not so positive, and not very relaxed afterwards. Thinking about your exercise prescription, please list the reasons or ways in which you, personally, might expect this exercise to lead to negative feelings, and what specifically about this exercise might make you, personally, feel bad."

Negative Affect Condition

Participants receive no information about affective response

Control Condition

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • eligible participants will be between the ages of 18 and 39 (for men) and 18 and 45 (for women)
  • free of overt disease (as cleared by clinical translational research center medical staff)
  • free of mental health conditions other than depression and anxiety (by self-report)
  • physically capable of engaging in moderate exercise activity (i.e., no injuries or physical impairments)
  • willing to receive a "prescription" for exercise intensity, frequency, and duration, and have access to a computer with Internet connectivity in order to complete the online follow-up survey.

You may not qualify if:

  • elite (i.e., paid) athletes or required to participate in aerobic exercise in conjunction with their occupation (e.g., aerobics instructors)
  • women must not be pregnant or planning to become pregnant during the study period
  • on any medications for which exercise is contraindicated (as cleared by clinical translational research center medical staff)
  • smoker

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Bethany Kwan, PhD

    University of Colorado School of Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 30, 2015

First Posted

September 25, 2015

Study Start

September 1, 2009

Primary Completion

January 1, 2010

Study Completion

February 1, 2010

Last Updated

September 25, 2015

Record last verified: 2015-09