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ExerciseNCT02615821

Mental Contrasting Physical Activity Study

A study testing Mental Contrasting in people with Exercise and Attitude to Health, run by University of British Columbia at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Given the numerous physical and psychological benefits of engaging in regular physical activity (Biddle \& Ekkekakis, 2005; Warburton et al., 2007) and the decrease in students' physical activity levels during the transition from high school to university (Bray \& Born, 2010) it is important for researchers to develop… Read more about this study

Who is it for?
Any age, women onlyHealthy volunteers can take part
Conditions the study is for
Exercise, Attitude to Health, Motivation
What is being tested?
Mental Contrasting
Could I receive a placebo?
No, everyone receives an active treatment
How many people
105 participants
Where
1 siteCanada
Study dates
Jan 2015to Nov 2015
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Individuals will be eligible to participate if they are female, inactive (i.e., engage in moderate-vigorous intensity physical activity for more than 30 minutes, less than three times a week), studying for an undergraduate degree at the University of British Columbia, and are able to read and converse in English.

Who cannot join

  • Participants will be excluded if they have any self-reported physical health conditions using the online version of the PAR-Q+ (http://eparmedx.com/?page_id=75) that would restrict them from increasing their physical activity behaviours at the time of the intervention.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Psychology of Exercise, Health, and Physical Activity Laboratory, University of British Columbia

    Vancouver, British Columbia, V6T 1Z1

Other trials in Canada

About this study

Given the numerous physical and psychological benefits of engaging in regular physical activity (Biddle \& Ekkekakis, 2005; Warburton et al., 2007) and the decrease in students' physical activity levels during the transition from high school to university (Bray \& Born, 2010) it is important for researchers to develop time-and-cost-effective interventions to prevent this drop in physical activity. Intervention research shows mental contrasting (a goal setting strategy) can be taught in a cost-and-time-effective way in order to increase physical activity (Oettingen, 2012). Researchers have also found that individuals who consider the emotional effects of physical activity are more likely to be physically active than those who consider the health-related effects (Rhodes et al., 2009). The purpose of this research is to combine these two approaches to develop and evaluate a novel mental contrasting intervention to increase physical activity among a sample of undergraduate students.

Read the detailed description

The transition from high school to university is a vulnerable period for discontinuing regular physical activity, which can have implications for individuals' physical and psychological health (Bray \& Born, 2010). Accordingly, it is imperative to find and implement cost and time-effective interventions to mitigate the consequences of this transition. Mental contrasting is a goal-setting strategy that involves imagining the greatest outcome associated with achievement of a desired future goal while considering the aspects of one's present situation that may serve as obstacles for attaining that same goal (Oettingen \& Gollwitzer, 2010). Intervention research has shown that mental contrasting can be taught as a metacognitive strategy in a cost- and time-effective way, affecting numerous health behaviours including physical activity (Oettingen, 2012). Drawing from diverse theoretical perspectives (e.g., Bechara, 2005; Lawton, Conner, \& McEachan, 2009; Williams, 2010), recent meta-analytic evidence suggests that affective judgements (e.g., enjoyable-unenjoyable) exert greater influence on physical activity behaviors than health-related instrumental judgements (e.g., useful-useless; Rhodes, Fiala, \& Conner, 2009). Nevertheless, research has yet to utilize mental contrasting as a means of targeting affective judgements, through intervention, in order to bolster physical activity promotion efforts. This research will examine how an affective mental contrasting intervention will change university students' affective judgements in comparison to instrumental mental contrasting and standard mental contrasting comparison conditions, and the subsequent impact of these changes on physical activity behaviour.

Being tested
Mental Contrasting
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mental ContrastingBehavioural

    n the mental contrasting activity participants will be asked by the researcher to consider the best outcome associated with engaging in physical activity, as well as the obstacles they may encounter while completing the activity. The first question will ask participants to name the most positive outcome of realizing their goal (e.g., feeling more awake during classes; weight loss). The second question will ask participants to name the most critical obstacle (e.g., feeling tired; rain) to reaching their goal.

Study groups in NCT02615821
Study groupRoleWhat they receive
Affective Mental ContrastingExperimentalBefore the goal formation or mental contrasting activities, participants will receive information about the affective benefits of exercising (e.g. regular physical activity has been shown to reduce stress, physical activity is enjoyable), and related research support including appropriate references. During the mental contrasting component of the activity the prompts will remain the same as the standard condition, with minor variations in questions in order to elicit affective judgements. Specifically, the affective condition will include the additional prompts "Why might you find exercise to be enjoyable, pleasant, exciting, or fun?" for eliciting outcomes, and "Why might you find exercise to be unenjoyable, unpleasant, boring, or miserable?" for eliciting obstacles.
Receives: Behavioral: Mental Contrasting
Instrumental Mental ContrastingActive comparatorBefore the goal formation or mental contrasting activities,participants will receive information about the instrumental benefits of exercising (e.g., regular physical activity reduces the risk of developing cancer) and related research support, again including appropriate references. During the mental contrasting component of the activity the prompts will remain the same as the standard condition, with minor variations in questions in order to elicit either instrumental judgements. Specifically, the instrumental conditions will include the prompts "Why might you find exercise to be useful, advantageous, beneficial, or important?" for eliciting outcomes, and "Why might you find exercise to be unimportant, useless, inconvenient, or detrimental?" for eliciting obstacles.
Receives: Behavioral: Mental Contrasting
Standard Mental ContrastingActive comparatorIn the standard condition, the space where the affective and instrumental benefits of physical activity were listed in the instrumental and affective conditions, will be left blank in the standard condition, and no additional prompting questions will be given, allowing for the idiosyncratic identification of obstacles and outcome.
Receives: Behavioral: Mental Contrasting

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change is accelerometry measured moderate-vigorous physical activity from baseline

    Actigraph accelerometers will measure daily activities. A standard 7-day accelerometry monitoring protocol will be used. Participants will also complete three one-week physical activity logs corresponding to the three accelerometry periods. In these logs, participants will record the time the monitor is on and off, in addition to recording all activities performed with or without the monitor.

    Measured: One week immediately following the intervention

  2. Change is accelerometry measured moderate-vigorous physical activity from baseline

    Actigraph accelerometers will measure daily activities. A standard 7-day accelerometry monitoring protocol will be used. Participants will also complete three one-week physical activity logs corresponding to the three accelerometry periods. In these logs, participants will record the time the monitor is on and off, in addition to recording all activities performed with or without the monitor.

    Measured: Four-week follow-up

Secondary outcomes (2)
  1. Change in Godin's Leisure Time Exercise Questionnaire (GLTEQ)

    Participants will report the typical number of minutes per week they engaged in mild, moderate, and vigorous physical activity. As per the protocol for scoring the GLTEQ, physical activity is transformed into MET hours by multiplying hours of engagement in mild physical activity by 2, moderate activity by 4, and vigorous physical activity by 7, and then summing these values to provide an estimate of MET hours/week for each of the two time points assessed.

    Measured: Change between baseline and four-week follow-up

  2. Change is Affective and Instrumental Physical Activity Judgements

    Instrumental and affective judgements towards participants' physical activity goal will be measured using semantic differential scales (Ajzen, 2002). Five items will be used to tap instrumental judgements (e.g. 'For me, engaging in moderate to vigorous aerobic physical activity for at least 150 minutes a week for the next 6 weeks would be': useless-useful), and five items will be used to tap affective judgements (e.g. 'For me, engaging in moderate to vigorous aerobic physical activity for at least 150 minutes a week for the next 6 weeks would be': unenjoyable-enjoyable). Each adjective pair will be rated on a 7-point unipolar scale (1-7) and a mean score will be computed for instrumental and affective subscales respectively.

    Measured: Changes between baseline, the week immediately following the intervention, and a four-week follow-up.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Nov 2015 (estimated)
  2. Study startJan 2015
  3. Primary completionNov 2015
  4. Study completionNov 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
105 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02615821
Sponsor's protocol ID
H14-02120
Status last verified
Nov 2015
First submitted
19 Nov 2015
Last updated
26 Nov 2015
Results posted
No

Publications

  • Ruissen GR, Rhodes RE, Crocker PRE, Beauchamp MR. Affective mental contrasting to enhance physical activity: A randomized controlled trial. Health Psychol. 2018 Jan;37(1):51-60. doi: 10.1037/hea0000551. Epub 2017 Oct 5.

    PubMed 28981303

Questions about this trial

What is this clinical trial studying?

A study testing Mental Contrasting in people with Exercise and Attitude to Health, run by University of British Columbia at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Nov 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change is accelerometry measured moderate-vigorous physical activity from baseline (time frame: One week immediately following the intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02615821, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Nov 2015.

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