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Affective Responses Following Aerobic Exercise With Different Intensities

NCT03081520 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2018-06-18

No results posted yet for this study

Summary

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.

Conditions

  • Health Behavior

Interventions

BEHAVIORAL

Affective response MIT

Examine acute affective responses during and after five sessions of endurance training with moderate intensity continuous training

BEHAVIORAL

Affective response HAIT

Examine acute affective responses during and after five sessions of endurance training with high-intensity aerobic interval training

BEHAVIORAL

Affective response HIIT

Examine acute affective responses during and after five sessions of endurance training with high-intensity sprint interval training

Sponsors & Collaborators

  • University of South-Eastern Norway

    lead OTHER

Principal Investigators

  • Solfrid Bratland-Sanda, PhD · University College of Southeast Norway

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-05
Primary Completion
2017-12-15
Completion
2017-12-15

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03081520 on ClinicalTrials.gov