Effects of Hiit Associated With Emotional Regulation on Negative Emotions

Sponsor
Federal University of Paraíba (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05508685
Collaborator
(none)
1
4
2

Study Details

Study Description

Brief Summary

Despite the benefits of physical exercise, the population does not adhere to the recommended levels of physical activity. The reported difficulties in starting and maintaining a physical exercise program are attributed to personal barriers and lack of motivation. Thus, there is an urgent need for efficient intervention proposals to increase engagement in daily physical exercise. High-intensity interval training (HIIT) is a promising and economical method, aiming at the development of efforts at high, maximum or supramaximal intensity, based on several methods: calisthenics (using the body's own strength) resistance (heavy objects, bars or devices for high-repetition resistance activities) and traditional (exercise modalities such as running and cycling). Emotional regulation (ER) is essential for the psychosocial well-being of human beings and is defined as the ability to influence, experience and express emotions, being an action, conscious or not, that directly modulates emotions and alters their nature as the intensity and duration. Regular physical exercise has been attributed to a reduction in depression symptoms, an increase in emotional well-being and a reduction in negative feelings. In addition to physical exercise, the use of cognitive reassessment to regulate emotions was positively associated with a decrease in negative affect in psychopathological diagnoses.

Condition or Disease Intervention/Treatment Phase
  • Other: HIIT and Cognitive Reassessment
  • Other: HIIT group
  • Other: Emotional regulation strategy group
  • Other: placebo group
N/A

Detailed Description

Main goal

To evaluate the effects of high-intensity interval training (HIIT) associated with a cognitive reassessment strategy on negative emotions in sedentary women.

Specific objectives

Evaluate and compare the positive and negative affective of women in three moments; Evaluate and compare the intensity and valence of emotions in three moments; Investigate possible associations between emotion dysregulation and emotion regulation strategies in positive and negative affect; Investigate and compare HIIT intensity and emotion regulation strategy in pleasure and displeasure during physical exercise during practice.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effects of Hiit Associated With Emotional Regulation on Negative Emotions
Anticipated Study Start Date :
Sep 30, 2022
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: HIIT and Cognitive Reassessment

The experimental group will receive high-intensity interval training associated with cognitive reassessment

Other: HIIT and Cognitive Reassessment
Participants will receive 40 minutes of high-intensity interval training focusing on the upper and lower limbs associated with a cognitive reassessment strategy during the exercises.

Active Comparator: HIIT Group

The HITT group will receive only the exercise without cognitive reassessment

Other: HIIT group
Participants will receive high-intensity interval training, lasting 40 minutes, focusing on upper and lower limbs.

Active Comparator: Emotional regulation strategy group

This group will receive only cognitive reassessment strategy

Other: Emotional regulation strategy group
Participants will be instructed to cognitively reassess the negative emotions they feel or do not feel during the practice of the exercises. Participants will receive instructions on how to reassess.

Placebo Comparator: Group No exercise and cognitive reassessment

This group will only be evaluated in pre and post, without intervention.

Other: placebo group
Participants in this group will not receive any intervention. Only pre and post experiment will be evaluated.

Outcome Measures

Primary Outcome Measures

  1. Positive and Negative Affect Scale [Fifteen days]

    Each item is rated on a five-point Likert scale, ranging from 1 = Very Slightly or Not at all to 5 = Extremely, to measure the extent to which affect was experienced in a specified period of time.

Secondary Outcome Measures

  1. Self Assessment Manikin [Fifteen days]

    The Self-Assessment Mannequin (SAM) is a non-verbal pictorial assessment technique that directly measures pleasure, arousal, and mastery associated with a person's affective reaction to a wide variety of stimuli. The reports are subjective to measure a series of images that varied in both valence and affective intensity.

  2. Feeling Scale [Fifteen days]

    The feeling scale was used to assess affective valence. The 11-point bipolar scale ranging from very bad (-5) to very good (+5), with anchors at Neutral (0) and all odd integers, including bad (-3), fairly bad (-1), reasonably good (+1) and good (+3).

  3. The Perceived Effort Scale [Fifteen days]

    Borg's Perceived Exertion Rating (RPE) is a way of measuring the intensity level of physical activity. These include a rating of 6 perceiving "no exertion" to 20 perceiving a "maximum exertion" of exertion. Practitioners generally agree that perceived exertion ratings between 12 and 14 on the Borg Scale suggest that physical activity is being performed at a moderate level of intensity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion criteria:

• No psychiatric or neurological disorder

Exclusion criteria:
  • Using mood-altering medications

  • Joint problems

  • Practicing physical activity for six months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Federal University of Paraíba

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Irinaldo Capitulino de Souza, principal investigator, Federal University of Paraíba
ClinicalTrials.gov Identifier:
NCT05508685
Other Study ID Numbers:
  • ICdesouza
First Posted:
Aug 19, 2022
Last Update Posted:
Aug 24, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Irinaldo Capitulino de Souza, principal investigator, Federal University of Paraíba

Study Results

No Results Posted as of Aug 24, 2022