Affective Responses Following Aerobic Exercise With Different Intensities

June 14, 2018 updated by: University of South-Eastern Norway
The aim of this study is to examine acute affective responses during and after a series of exercise sessions with different intensities in young healthy adults. The study is a randomized controlled trial with three different groups (A: moderate continuous training (MIT), B: high-intensity aerobe interval training (HAIT), C: high-intensity sprint interval training (HIIT)). Healthy adults aged 18-40 years (n=30) will be invited to participate. Each participant will perform a VO2max test followed by five session of the randomized type of training. The sessions will be completed within two weeks. The participants will complete questionnaires regarding exercise motivation (Behavioral Regulation of Exercise Questionnaire), mood (Positive and Negative Affect Scale, Profile of Mood States, Visual Analogue scale, Self-assessment Manikin Rating Scale) and perceived exhaustion (Borg Ratings of Perceived Exertion scale). In addition, blood lactate and heart rate will be obtained during and after each session.

Study Overview

Detailed Description

Physical activity has is considered as one of the most important health related aspects of the 21st century. In Norway, large epidemiological studies show that only about 30% of the adult population meet the physical activity recommendations of 150 minutes per week with moderate-to-vigorous intensity physical activity. Also, studies show that there are large dropout rates from lifestyle interventions, and that approximately 50% drop out from physical activity interventions within 6 months after start. One explanation for the dropout is performance of exercise with too vigorous intensities.

Very vigorous intensity physical activity can be experienced as unpleasant. According to the dual-mode theory there are positive affective responses after low-to-moderate intensity physical activity, whereas vigorous intensity physical activity trigger negative affective responses which again can lead to reduced motivation for the exercise. Unfortunately, many of the studies performed on affective responses to exercise have used one session only. The studies who have examined changes in affective responses after series of exercise have used vigorous intensities above the anaerobic threshold, and it is therefore unknown whether similar affective responses occur in vigorous intensity aerobe exercise.

The aim of this study is to examine acute affective responses during and after a series of exercise sessions with different intensities in young healthy adults.

To examine this, a randomized controlled clinical trial with three different groups (moderate intensity training (MIT), high-intensity aerobic interval training (HAIT) and high-intensity sprint interval training (HIIT)) will be conducted. A power calculation showed need for recruitment of 30 participants. The sample will consist of healthy young adults. All participants will perform one VO2max test, and five sessions with the intensity they are randomized to. All six sessions (test + exercise sessions) will be conducted within two weeks.

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Telemark
      • Bø, Telemark, Norway, 3800
        • University College of Southeast Norway

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy
  • No high intensity interval training during the past three months prior to participation
  • Regular exercise up to two sessions per week
  • 18-40 years of age
  • BMI <30 kg/m2

Exclusion Criteria:

  • Competing athlete
  • Smoker
  • Injury not compatible with performing the exercises
  • BMI <16 kg/m2
  • Pregnant

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Affective response MIT
Moderate intensity continuous training 50 min with walking or running on approximately 75% of HRmax
Examine acute affective responses during and after five sessions of endurance training with moderate intensity continuous training
Experimental: Affective response HAIT
High-Intensity Aerobic Interval Training 4x4 min with walking or running on 85-95% of HRmax 3 min active recovery between sets, intensity of approximately 70% of HRmax
Examine acute affective responses during and after five sessions of endurance training with high-intensity aerobic interval training
Experimental: Affective response HIIT
High-Intensity Interval Training 4-6 x 30-sec sprints on tread mill, >95% HRmax during sprints 4 min recovery between sprints, intensity of approximately 70% of HRmax
Examine acute affective responses during and after five sessions of endurance training with high-intensity sprint interval training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in self rated well-being rated on a Visual Analogue Scale
Time Frame: Two weeks
well-being rated on a Visual Analogue Scale
Two weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported change in affects using Positive and Negative Affect Scale
Time Frame: Two weeks
Positive and Negative Affect Scale
Two weeks
Self-reported change in physical activity motivation using Behavioural Regulation of Exercise Questionnaire - 2
Time Frame: Two weeks
Behavioural Regulation of Exercise Questionnaire - 2
Two weeks
Self-reported change in affective responses using Self-Assessment Manikin Rating Scale
Time Frame: Two weeks
Self-Assessment Manikin Rating Scale
Two weeks
Self-reported change in mood using scale Profile of Mood States
Time Frame: Two weeks
Use of the standardized and validated scale Profile of Mood States
Two weeks
Perceived exercise intensity during each exercise session using Borgs Ratings of Perceived Exertion (RPE) scale (6-20)
Time Frame: At minutes 0,10, 20, 40 and 50 in each exercise session
Borgs RPE scale (6-20)
At minutes 0,10, 20, 40 and 50 in each exercise session
Lactate during each exercise session (mMol/l)
Time Frame: At minutes 0,10, 20, 40 and 50 in each exercise session
Blood lactate samples (mMol/l)
At minutes 0,10, 20, 40 and 50 in each exercise session

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Solfrid Bratland-Sanda, PhD, University College of Southeast Norway

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 5, 2017

Primary Completion (Actual)

December 15, 2017

Study Completion (Actual)

December 15, 2017

Study Registration Dates

First Submitted

March 7, 2017

First Submitted That Met QC Criteria

March 15, 2017

First Posted (Actual)

March 16, 2017

Study Record Updates

Last Update Posted (Actual)

June 18, 2018

Last Update Submitted That Met QC Criteria

June 14, 2018

Last Verified

July 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • Affective responses exercise

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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