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AcAdeMiC: Acting With Acceptance, Mindfulness and Compassion to Overcome Test/Exam Anxiety (AcAdeMiC)

Primary Purpose

Adolescents, Test Anxiety

Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Intervention program for test anxiety
Sponsored by
University of Coimbra
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adolescents focused on measuring test anxiety, adolescents, acceptance, mindfulness, compassion

Eligibility Criteria

13 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • provision of written informed consent by participants and their legal guardians;
  • presence of high levels of test anxiety, confirmed through self-report assessment and clinical interview;
  • educational level from 9th to 12th grade;
  • absence of Neurodevelopmental Disorders, except Specific Learning Disorders of mild severity;
  • absence of any degree of cognitive decline or impairment;
  • absence of any severe Depressive Disorder;
  • absence of any other severe psychiatric condition (e.g., Obsessive-Compulsive Disorder, Bipolar Disorder, Psychotic Disorders);
  • not being under treatment for a psychiatric condition.

Exclusion Criteria:

  • no provision of written informed consent by participants and their legal guardians;
  • absence of high levels of test anxiety, confirmed through self-report assessment;
  • educational level below 9th and above 12th grade;
  • presence of Neurodevelopmental Disorders, except Specific Learning Disorders of mild severity;
  • presence of any degree of cognitive decline or impairment;
  • presence of any severe Depressive Disorder;
  • presence of any other severe psychiatric condition (e.g., Obsessive-Compulsive Disorder, Bipolar Disorder, Psychotic Disorders);
  • being under treatment for a psychiatric condition.

Sites / Locations

  • University of Coimbra

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention program for test anxiety

Control

Arm Description

12 weekly ICT-delivered individual sessions.

Waiting list that will have access to the intervention program after the 6-month follow-up assessment.

Outcomes

Primary Outcome Measures

Test Anxiety
Reactions to Tests for Adolescents (RT-A). Participants rate the items on a Likert scale from 1 to 4. Lower scores indicate a better outcome

Secondary Outcome Measures

General well-being
Mental Health Continuum - Short Form - for Youth (MHC-SF). Participants rate the items on a Likert scale from 0 to 5. Higher scores indicate a better outcome
School-related well-being
School-related Well-Being Scale (SWBS). Participants rate the items on a Likert scale from 1 to 5. Higher scores indicate a better outcome
Psychological flexibility in test situations
Test Anxiety Acceptance and Action Questionnaire for Adolescents (TA-AAQ-A). Participants rate the items on a Likert scale from 1 to 7. Higher scores indicate a better outcome
General psychological flexibility
Avoidance and Fusion Questionnaire for Youth (AFQ-Y). Participants rate the items on a Likert scale from 0 to 4. Lower scores indicate a better outcome
Mindfulness
Child and Adolescent Mindfulness Measure (CAMM). Participants rate the items on a Likert scale from 0 to 4. Higher scores indicate a better outcome
Self-compassion
Self-Compassion Scale (SCS-A). Participants rate the items on a Likert scale from 1 to 5. Higher scores indicate a better outcome

Full Information

First Posted
April 22, 2021
Last Updated
December 1, 2022
Sponsor
University of Coimbra
Collaborators
Fundação para a Ciência e a Tecnologia, CINEICC - Center for Research in Neuropsychology and Cognitive Behavioral Intervention
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1. Study Identification

Unique Protocol Identification Number
NCT04861116
Brief Title
AcAdeMiC: Acting With Acceptance, Mindfulness and Compassion to Overcome Test/Exam Anxiety
Acronym
AcAdeMiC
Official Title
AcAdeMiC: Acting With Acceptance, Mindfulness and Compassion to Overcome Test/Exam Anxiety - An ICT-based Psychotherapeutic Intervention for Adolescents
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
March 15, 2021 (Actual)
Primary Completion Date
July 31, 2022 (Actual)
Study Completion Date
July 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Coimbra
Collaborators
Fundação para a Ciência e a Tecnologia, CINEICC - Center for Research in Neuropsychology and Cognitive Behavioral Intervention

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Test Anxiety is a highly prevalent and impairing condition in adolescents (i.e., 9th to 12th grade students), significantly impacting on their mental health and well-being. Among Portuguese university students, test anxiety is the primary reason for seeking specialized psychological support, suggesting the importance of early intervention. Test anxiety associates to low self-compassion, acceptance and mindfulness, which have been increasingly acknowledged in literature as important processes to cultivate towards human experience and suffering, within intervention programs, particularly in adolescence, and in anxiety and fear of failure in academic settings. These processes are covered and enhanced within comprehensive models and evidence-based therapies that adopt an integrative, contextual and biopsychosocial approach, such as Acceptance and Commitment Therapy (ACT), and Mindfulness-Based Cognitive Therapy (MBCT), as well as an evolutionary approach, such as Compassion Focused Therapy (CFT). These approaches focus on receiving internal events (e.g., thoughts, emotions, memories) in an accepting and compassionate way, as part of human experience, without changing them, while developing a sense of vitality, well-being and commitment to valued ends in life, instead of focusing solely or mainly on symptom reduction (although it is usually a consequent outcome). However, there are no empirically validated therapeutic programs for adolescents with test anxiety promoting these processes combined. ICT-based interventions are accessible, convenient, cost-effective and have been proved effective in reducing anxiety disorders' symptomatology. Even though there are some empirically validated online interventions for test anxiety in adolescents, having shown promising results, these were mainly self-help/module-based programs, without a clinician facilitating the intervention. This project aims to develop and implement a 12-week ICT-based targeted, facilitated and manualized individual intervention for adolescent students, developing compassion, acceptance and mindfulness, in order to help improve test anxiety's regulation (and consequently symptom reduction), as well as increase general and school-related well-being, while promoting valued life action.
Detailed Description
All ethical and deontological requirements are guarenteed in this study. A sample of adolescent students (from 9th to 12th grade) is being online-recruited, through social media and contacts with Executive Boards of Portuguese secondary schools, private practices and study centers, advertising the study. Parents/legal guardians are encouraged to contact the team. From this approach, parents/legal guardians and respective adolescents who demonstrate interest are explained the aims and procedures of the study and asked to sign a written consent form. Adolescents are then assessed for eligibility through a test anxiety self-report measure and a clinical interview. Eligible participants will be randomly assigned to either an experimental group, who will reveive the intervention (facilitated by licenced psychotherapists with training in contextual therapies and are familiar with the intervention protocol), or a waiting-list control group, who will have access to the intervention after the six-month follow-up assessment. Both groups will complete a protocol with self-report measures, assessing psychopathology indicators, emotion regulation processes, and general and school-related well-being, in four different moments: at baseline (M0), immediatly after the intervention (M1), three months (M2) and six months (M3) after the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescents, Test Anxiety
Keywords
test anxiety, adolescents, acceptance, mindfulness, compassion

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention program for test anxiety
Arm Type
Experimental
Arm Description
12 weekly ICT-delivered individual sessions.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Waiting list that will have access to the intervention program after the 6-month follow-up assessment.
Intervention Type
Behavioral
Intervention Name(s)
Intervention program for test anxiety
Other Intervention Name(s)
AcAdeMiC: Acting With Acceptance, Mindfulness and Compassion to Overcome Test/Exam Anxiety
Intervention Description
12-week ICT-based manualized, targeted and facilitated individual intervention for adolescent students, that aims to promote compassion, acceptance and mindfulness, in order to help improve test anxiety's regulation (and consequently symptom reduction), as well as increase general and school-related well-being, while promoting valued life action.
Primary Outcome Measure Information:
Title
Test Anxiety
Description
Reactions to Tests for Adolescents (RT-A). Participants rate the items on a Likert scale from 1 to 4. Lower scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Secondary Outcome Measure Information:
Title
General well-being
Description
Mental Health Continuum - Short Form - for Youth (MHC-SF). Participants rate the items on a Likert scale from 0 to 5. Higher scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
School-related well-being
Description
School-related Well-Being Scale (SWBS). Participants rate the items on a Likert scale from 1 to 5. Higher scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
Psychological flexibility in test situations
Description
Test Anxiety Acceptance and Action Questionnaire for Adolescents (TA-AAQ-A). Participants rate the items on a Likert scale from 1 to 7. Higher scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
General psychological flexibility
Description
Avoidance and Fusion Questionnaire for Youth (AFQ-Y). Participants rate the items on a Likert scale from 0 to 4. Lower scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
Mindfulness
Description
Child and Adolescent Mindfulness Measure (CAMM). Participants rate the items on a Likert scale from 0 to 4. Higher scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
Self-compassion
Description
Self-Compassion Scale (SCS-A). Participants rate the items on a Likert scale from 1 to 5. Higher scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Other Pre-specified Outcome Measures:
Title
Depression, anxiety and stress
Description
Depression Anxiety and Stress Scales (DASS-21). Participants rate the items on a Likert scale from 0 to 3. Lower scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
Self-criticism
Description
Forms of Self-Criticizing/attacking and self-Reassuring Scale (FSCRS-A). Participants rate the items on a Likert scale from 0 to 4. Lower scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]
Title
Shame
Description
External and Internal Shame Scale for adolescents (EISS-A). Participants rate the items on a Likert scale from 0 to 4. Lower scores indicate a better outcome
Time Frame
6 months [From Baseline to 6 months follow-up]

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: provision of written informed consent by participants and their legal guardians; presence of high levels of test anxiety, confirmed through self-report assessment and clinical interview; educational level from 9th to 12th grade; absence of Neurodevelopmental Disorders, except Specific Learning Disorders of mild severity; absence of any degree of cognitive decline or impairment; absence of any severe Depressive Disorder; absence of any other severe psychiatric condition (e.g., Obsessive-Compulsive Disorder, Bipolar Disorder, Psychotic Disorders); not being under treatment for a psychiatric condition. Exclusion Criteria: no provision of written informed consent by participants and their legal guardians; absence of high levels of test anxiety, confirmed through self-report assessment; educational level below 9th and above 12th grade; presence of Neurodevelopmental Disorders, except Specific Learning Disorders of mild severity; presence of any degree of cognitive decline or impairment; presence of any severe Depressive Disorder; presence of any other severe psychiatric condition (e.g., Obsessive-Compulsive Disorder, Bipolar Disorder, Psychotic Disorders); being under treatment for a psychiatric condition.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cláudia P. Pires, M.Sc.
Organizational Affiliation
University of Coimbra
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Coimbra
City
Coimbra
ZIP/Postal Code
3000-115
Country
Portugal

12. IPD Sharing Statement

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