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Completed

NCT Number: NCT03047590

Comparison of Affect-based, Self-selected, and Traditional Exercise Prescriptions

This study will evaluate adherence to four types of walking programs. Participants will be randomized to walking programs that included either (1) affect-based exercise intensity, (2) self-selected (or "choice-based") exercise intensity, (3) heart-rate based exercise intensity, or (4) heart-rate guided exercise intensity with the emphasis on affective benefits.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Duke University IBRC Lab

Durham, North Carolina, 27701, United States

About this study

The purpose of this study is to determine if an "affect-based" or "choice-based" exercise prescription is more effective for behavior change than a traditional, "moderate-intensity" exercise prescription. Prior research suggests that "choice-based" or "self-selected" exercise intensity is more pleasant and adhered to than "moderate-intensity exercise" (Williams et al., 2014). Similarly, affect-based exercise prescriptions (i.e., an exercise prescription where intensity is regulated based on the pleasure-displeasure one feels while exercising) appear to have merit (Baldwin, Kangas, Denman, Smits, Yamada, & Otto, 2016).

However, choice-based and affect-based exercise prescriptions have not been compared to each other. Further, it is unknown if it is the intensity regulation that matters (e.g., "choose an intensity that feels good" or the focus on affect (e.g., "focus on feeling good). Third, prior research has not objectively measured physical activity behavior.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Must be fluent in English
  • Must be able to walk
  • Exercise less than 90 minutes per week at a moderate-intensity
  • Must be able to attend laboratory visits
  • Must have mobile internet accent and a personal smartphone (iPhone iOS 9+ or Android OS 4.3+)
  • Can safely exercise at an intensity that is at least "moderate"

Exclusion criteria

  • People who are recommended to have medical clearance prior to exercising, according to the American College of Sports Medicine's preparticipation screening criteria, will be excluded

Treatment and study plan

Choice-based Exercise Intensity

Behavioral

Participants are instructed to choose whichever intensity they want, rather than regulate their intensity based on heart rate.

Positive Affect Focus

Behavioral

Participants are instructed to focus on feeling good while exercising.

Heart rate-based Exercise Intensity

Behavioral

Participants are instructed to regulate their exercise intensity based on their heart rate.

Primary outcomes

  1. Change in objectively measured exercise behavior

    Time frame: This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)

    Minutes per week of objectively measured exercise behavior.

Secondary outcomes

  1. Change in self-reported exercise behavior

    Time frame: This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)

    Minutes per week of self-reported exercise behavior that is reported using exercise log.

  2. Change in affective attitudes

    Time frame: Measured during baseline assessment period and at the end of the intervention

    Affective attitudes toward exercise

  3. Self-reported intrinsic motivation (questionnaires)

    Time frame: Two weeks into study intervention

    Intrinsic motivation for exercise program

  4. Enjoyment

    Time frame: Measured at the end of the intervention period (4 weeks)

    Enjoyment of exercise program.

  5. Change in weight

    Time frame: Measured at the beginning and end of the study (6 weeks).

    Body weight

  6. Change in resting heart rate

    Time frame: Measured at the beginning and end of the study (6 weeks).

    Resting heart rate

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Feb 9, 2017
Registry last updated
Jul 9, 2018

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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