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Clinical Trials/NCT05694468
NCT05694468CompletedNot Applicable

The Effects of a Relaxation Intervention on College Students' Social-emotional Competence: A Mixed Methods Approach

University of Évora2 sites in 1 country20 target enrollmentStarted: March 22, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
20
Locations
2
Primary Endpoint
Personal and professional development

Study Overview

Brief Summary

Objective: To examine the impact of a psychomotor relaxation program on college students' social-emotional competence, personal and professional development. Participants: Twenty female college students participated. Methods: In this non-random one-group repeated measures study with a mixed approach (quantitative and qualitative analysis), participants were tested on two occasions 4 weeks apart (baseline measure), and then engaged in the psychomotor relaxation program twice weekly for 8 weeks. Participants were tested again after the intervention program (post-test).

Detailed Description

This was a non-random one-group repeated measures study with a mixed approach (quantitative and qualitative analysis), where participants served as their own controls.

The investigators examined the chronic effects of the intervention program, collecting the instruments online at week 1 (pretest 1) and week 5 (pretest 2), to establish the baseline measures, and at the end of the 8-week period (post-test). In the post-test evaluation, participants also completed the questionnaire with open-ended questions. Investigators also measured salivary cortisol at the beginning and end of the 1st and the 15th sessions to evaluate the acute effects of the intervention program.

Students participated in a psychomotor relaxation program comprised by two 20-minute sessions per week for 8 weeks, combining body awareness, muscle tone regulation and breathing exercises

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • age between 18 and 30 years old
  • not having participated in a similar intervention program within the last 6 months
  • not have a physical condition that can affect participation in the program
  • do not take medication that can influence the studied outcomes.

Exclusion Criteria

  • age under 18 or over 30 years old
  • have participated in a similar intervention program within the last 6 months
  • have a physical condition that can affect participation in the program
  • take medication that can influence the studied outcomes.

Outcomes

Primary Outcomes

Personal and professional development

Time Frame: 1 day (after the intervention program)

A questionnaire was created to the present study comprising 3 open-ended questions concerning the perception of the students about the influence of the intervention program on their personal development, and the benefits that the intervention program may have in the exercise of their future profession as an early childhood educator.

Cortisol levels

Time Frame: 2 days

Cortisol levels (mcg/dL) were quantified in saliva samples collected at the same time and in the same place where the intervention occurred. Before and after the 1st and 15th session, the samples were collected directly from each participant's mouth.

Change in Affective states

Time Frame: 1, 4 and 12 weeks.

Affective states were measured through the Portuguese short version of the Profile of Mood States (POMS).

Change in Stress

Time Frame: 1, 4 and 12 weeks.

Stress was measured through the Portuguese version of the Perceived Stress Scale (PSS-10).

Change in Psychological wellbeing

Time Frame: 1, 4 and 12 weeks.

Psychological wellbeing was measured through the Portuguese short version of the Scales of Psychological Wellbeing (EBEP).

Change in Interoceptive awareness

Time Frame: 1, 4 and 12 weeks.

Interoceptive awareness was measured through the Portuguese version of the Multidimensional Assessment of Interoceptive Awareness (MAIA).

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University of Évora
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Andreia Dias Rodrigues

Principal Investigator

University of Évora

Study Sites (2)

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