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Exploring the Efficacy of Treatments for Anxiety and Depression Among College Students

Primary Purpose

Anxiety, Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
External Qigong
Mindfulness Meditation
Psychoeducation
Sponsored by
University of South Dakota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 18 years or older. Currently enrolled in a two or four-year college. English speaking. Willing to travel to the study location. Access to a computer or smartphone with a Wifi connection. Score of a three or higher on the Generalized Anxiety Disorder 2-item and/or score of a three or higher on the Patient Health Questionnaire-2. Exclusion Criteria: Not currently enrolled in college. Not able to travel to the study location. No access to a computer or smartphone with Wifi. Score < 3 on the Generalized Anxiety Disorder-2 and < 3 on the Patient Health Questionnaire-2.

Sites / Locations

  • University of South Dakota

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

External Qigong

Mindfulness Meditation

Psychoeducation

Arm Description

Participants will meet individually with the Qigong practitioner once a week for three weeks for 30-minute segments.

Participants will meet individually with the mindfulness practitioner once a week for three weeks for 30-minute segments.

In the psychoeducation arm, participants will receive recordings online, once a week for three weeks which will be approximately 30 minutes in length.

Outcomes

Primary Outcome Measures

Anxiety
Symptoms of anxiety will be assessed through a trait anxiety assessment (State-Trait-Anxiety Inventory). The range of possible scores spans from a minimum score of 20 to a maximum score of 80 - the higher the score, the higher the symptoms of anxiety.
Depression
Symptoms of depression will be assessed through a trait depression assessment (Beck Depression Inventory). Scores from the Beck Depression Inventory range from 0-63, with higher scores representing high depression levels.

Secondary Outcome Measures

Intention to persist in college
Change in participants' intention to persist in college will be assessed through an individual item rated in a numeric rating scale. Scores range from 0 to 5 with higher scores reflecting greater intent to remain in college.
Anxiety
Symptoms will be assessed through a state anxiety assessment. Scores range from 0-60 with higher scores indicating higher levels of anxiety.
Depression
Symptoms will be assessed through a state depression assessment. Scores range from 0-20 with higher scores indicating higher levels of depression.

Full Information

First Posted
April 19, 2023
Last Updated
August 25, 2023
Sponsor
University of South Dakota
Collaborators
Subtle Energy Funders Collective
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1. Study Identification

Unique Protocol Identification Number
NCT06013930
Brief Title
Exploring the Efficacy of Treatments for Anxiety and Depression Among College Students
Official Title
Exploring the Efficacy of Alternative Treatments for Depression and Anxiety Among College Students: A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2023 (Anticipated)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Dakota
Collaborators
Subtle Energy Funders Collective

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
The goal of this randomized control group is to learn about effective treatments for college students experiencing anxiety and/or depression. The main questions this clinical trial aims to answer are: 1) Can alternative treatments decrease anxiety and/or depression among college students? 2) Can alternative treatments increase retention rates among college students experiencing anxiety and/or depression? Participants will be randomly assigned to one of three intervention groups: external qigong, mindfulness meditation, or psychoeducation. Researchers will compare outcomes from each group to explore treatment differences.
Detailed Description
Method/Design. This study will be a single-site, three-arm, randomized, controlled trial. College students (N=51) with elevated depression and/or anxiety will be randomized to either external qigong (EQ), mindfulness meditation (MM), or psychoeducation (PE). Each intervention will be applied for 30 minutes, once a week for three weeks in a community setting. The co-primary outcomes, depression and anxiety, and the secondary outcome, intention to persist in college, will be assessed by a blinded researcher at baseline, one-week post treatment, and one-month follow-up. Change in sense of connection during the treatment session, measured with a comprehensive battery of self-report indices, will be the primary therapeutic mechanism. Aims and Objectives. The proposed project's central hypothesis is that EQ will increase students' mental health and intention to persist in college by balancing the flow of energy in their bodies. Aim 1. Examine EQ's acceptability in a sample of college students with depression and/or anxiety. Hypothesis: Student retention (i.e., attendance in both treatment sessions) and self-reported treatment acceptability will be better for EQ relative to PE. EQ and MM will demonstrate equivalent acceptability. Aim 2. Determine EQ's effect on anxiety, depression (co-primary outcomes), and intention to persist in college (secondary outcome) over time. Hypothesis: EQ will decrease depression and anxiety while increasing intention to persist in college relative to PE from baseline to one-month follow-up. The co-primary and secondary outcome scores will not differ between EQ and MM. Aim 3. Investigate EQ's immediate effect on students' sense of connection (therapeutic mechanism). Hypothesis: EQ will increase students' sense of connection relative to PE during the treatment sessions. EQ and MM will have equivalent effects on sense of connection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to receive either: 1) External Qigong, 2) Mindfulness Meditation, or 3) Psychoeducation.
Masking
Outcomes Assessor
Masking Description
The PI will randomly assign participants to condition and coordinate treatment group scheduling; the assessor will be blinded to condition.
Allocation
Randomized
Enrollment
51 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
External Qigong
Arm Type
Experimental
Arm Description
Participants will meet individually with the Qigong practitioner once a week for three weeks for 30-minute segments.
Arm Title
Mindfulness Meditation
Arm Type
Experimental
Arm Description
Participants will meet individually with the mindfulness practitioner once a week for three weeks for 30-minute segments.
Arm Title
Psychoeducation
Arm Type
Active Comparator
Arm Description
In the psychoeducation arm, participants will receive recordings online, once a week for three weeks which will be approximately 30 minutes in length.
Intervention Type
Behavioral
Intervention Name(s)
External Qigong
Intervention Description
External Qigong will be facilitated by a seasoned Qigong practitioner. The Qigong practitioner will assist participants in learning how to use the healing powers of their bodies to decrease feelings of anxiety and/or depression
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Meditation
Intervention Description
Mindfulness meditation will be facilitated by a seasoned mindfulness practitioner. Participants will be guided through a meditation designed to help increase a sense of interconnectedness among their college community. They will also learn how to deconstruct feelings of anxiety and/or depression into sensory, emotional, cognitive, and behavioral components.
Intervention Type
Other
Intervention Name(s)
Psychoeducation
Intervention Description
In the psychoeducation arm, participants will receive information related to managing anxiety and/or depression through a recorded presentation. Participants will learn about stress-management techniques to help reduce symptoms of anxiety and/or depression. They will also receive information on resources that could be helpful in treating anxiety and/or depression.
Primary Outcome Measure Information:
Title
Anxiety
Description
Symptoms of anxiety will be assessed through a trait anxiety assessment (State-Trait-Anxiety Inventory). The range of possible scores spans from a minimum score of 20 to a maximum score of 80 - the higher the score, the higher the symptoms of anxiety.
Time Frame
Change from baseline assessment, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Depression
Description
Symptoms of depression will be assessed through a trait depression assessment (Beck Depression Inventory). Scores from the Beck Depression Inventory range from 0-63, with higher scores representing high depression levels.
Time Frame
Change from baseline assessment, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Secondary Outcome Measure Information:
Title
Intention to persist in college
Description
Change in participants' intention to persist in college will be assessed through an individual item rated in a numeric rating scale. Scores range from 0 to 5 with higher scores reflecting greater intent to remain in college.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Anxiety
Description
Symptoms will be assessed through a state anxiety assessment. Scores range from 0-60 with higher scores indicating higher levels of anxiety.
Time Frame
Changes in participant's state anxiety will be captured within 5-minutes prior to each intervention and within 5 minutes after each intervention (mindfulness, external qigong, and psychoeducation).
Title
Depression
Description
Symptoms will be assessed through a state depression assessment. Scores range from 0-20 with higher scores indicating higher levels of depression.
Time Frame
Changes in participant's state depression will be captured within 5-minutes prior to each intervention and within 5 minutes after each intervention (mindfulness, external qigong, and psychoeducation).
Other Pre-specified Outcome Measures:
Title
Adverse Childhood Experiences questionnaire.
Description
Participants adverse childhood experiences will be assessed at baseline to explore how childhood adversities moderate outcomes.The ACEs questionnaire was adapted from the Felitti et al., (1998) wave two survey and current questions used by the CDC's telephone Behavioral Risk Factor Surveillance System survey collected in all 50 states. ACES range between 0-13 and the higher the score, the higher the number of ACES.
Time Frame
Baseline
Title
Sensation Manikin
Description
Change in the distribution of pleasant and unpleasant bodily sensations. Scores can range from 0-100 for pleasant (higher scores indicate higher pleasant feelings) and 0-100 for unpleasant feelings (higher scores indicate higher levels of unpleasant sensations).
Time Frame
Changes in participant's state body sensations will be captured within 5-minutes prior to each intervention and within 5 minutes after each intervention (mindfulness, external qigong, and psychoeducation).
Title
Trait Self-Transcendence
Description
Change in trait self-transcendence from baseline through 3-month follow-up will be assessed with the Nondual Awareness Dimensional Assessment - Trait Version. Scores range from 0 to 52, with higher scores reflecting greater trait self-transcendence.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Self-Transcendent State
Description
Change in self-transcendent state will be measured with the Nondual Awareness Dimensional Assessment - State Version. Scores range from 0 to 10, with higher scores reflecting greater self-transcendence.
Time Frame
Changes in participant's self-transcendence will be captured within 5-minutes prior to each intervention and within 5 minutes after each intervention (mindfulness, external qigong, and psychoeducation).
Title
Perceived Discrimination
Description
Changes in the perception of experiencing discrimination (Everyday Discrimination). Scores range from 0 -54 with higher scores indicating higher levels of discrimination.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Connectedness to Nature Questionnaire
Description
The effects on Connectedness to Nature as a moderator between treatment and outcomes. The scale consists of 16 items rated on a 5-point Likert scale, from 1 (strongly disagree) to 5 (strongly agree) and is scored by creating a mean of the 16 items, with scores ranging from one to five, with higher scores indicating a stronger connectedness to nature than lower scores.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Dispositional Mindfulness Scale
Description
The Metacognitive Processes of Decentering scale (MPoD-t) will be used to assess the effects of dispositional mindfulness as a moderator between treatment and outcomes. Scores range from 0-80 with higher scores indicating higher dispositional mindfulness.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).
Title
Sense of Belonging in College
Description
The role of treatment type on the participant's sense of belonging in college. Scores range from 0-56 with higher scores indicating higher levels of belonging.
Time Frame
Baseline, post treatment (one week after the final treatment session), and follow-up (one month after the final treatment session).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years or older. Currently enrolled in a two or four-year college. English speaking. Willing to travel to the study location. Access to a computer or smartphone with a Wifi connection. Score of a three or higher on the Generalized Anxiety Disorder 2-item and/or score of a three or higher on the Patient Health Questionnaire-2. Exclusion Criteria: Not currently enrolled in college. Not able to travel to the study location. No access to a computer or smartphone with Wifi. Score < 3 on the Generalized Anxiety Disorder-2 and < 3 on the Patient Health Questionnaire-2.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Natalie Lecy, PhD
Phone
6058644151
Email
natalie.lecy@usd.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Natalie Lecy, PhD
Organizational Affiliation
Assistant Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of South Dakota
City
Sioux Falls
State/Province
South Dakota
ZIP/Postal Code
57107
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Natalie Lecy, PhD
Phone
801-910-3165
Email
natalie.lecy@usd.edu
First Name & Middle Initial & Last Name & Degree
Natalie Lecy, Phd

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
11597055
Citation
Steer RA, Brown GK, Beck AT, Sanderson WC. Mean Beck Depression Inventory-II scores by severity of major depressive episode. Psychol Rep. 2001 Jun;88(3 Pt 2):1075-6. doi: 10.2466/pr0.2001.88.3c.1075.
Results Reference
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PubMed Identifier
31246748
Citation
Hanley AW, Garland EL. Mapping the Affective Dimension of Embodiment With the Sensation Manikin: Validation Among Chronic Pain Patients and Modification by Mindfulness-Oriented Recovery Enhancement. Psychosom Med. 2019 Sep;81(7):612-621. doi: 10.1097/PSY.0000000000000725.
Results Reference
background
PubMed Identifier
30058824
Citation
Hanley AW, Nakamura Y, Garland EL. The Nondual Awareness Dimensional Assessment (NADA): New tools to assess nondual traits and states of consciousness occurring within and beyond the context of meditation. Psychol Assess. 2018 Dec;30(12):1625-1639. doi: 10.1037/pas0000615. Epub 2018 Jul 30.
Results Reference
background
PubMed Identifier
33091745
Citation
Knowles KA, Olatunji BO. Specificity of trait anxiety in anxiety and depression: Meta-analysis of the State-Trait Anxiety Inventory. Clin Psychol Rev. 2020 Dec;82:101928. doi: 10.1016/j.cpr.2020.101928. Epub 2020 Oct 10.
Results Reference
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PubMed Identifier
19341164
Citation
Sims M, Wyatt SB, Gutierrez ML, Taylor HA, Williams DR. Development and psychometric testing of a multidimensional instrument of perceived discrimination among African Americans in the Jackson Heart Study. Ethn Dis. 2009 Winter;19(1):56-64.
Results Reference
background
PubMed Identifier
9635069
Citation
Felitti VJ, Anda RF, Nordenberg D, Williamson DF, Spitz AM, Edwards V, Koss MP, Marks JS. Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. Am J Prev Med. 1998 May;14(4):245-58. doi: 10.1016/s0749-3797(98)00017-8.
Results Reference
background
PubMed Identifier
29312052
Citation
Navarro O, Olivos P, Fleury-Bahi G. "Connectedness to Nature Scale": Validity and Reliability in the French Context. Front Psychol. 2017 Dec 12;8:2180. doi: 10.3389/fpsyg.2017.02180. eCollection 2017.
Results Reference
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Exploring the Efficacy of Treatments for Anxiety and Depression Among College Students

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