ClinicalTrials.gg
CompletedNCT07813520ACTUpdated Sep 10, 2026

Effect of an ACT-based Intervention to Reduce Anxiety in Medical Students

An interventional study of ACT_based intervention and Active Control group in Anxiety, Somatization and Depressive Symptom, sponsored by University of Guadalajara. Completed at 1 site in Mexico. Open to participants aged 18 Years to 26 Years. Per ClinicalTrials.gov, last updated 2026-09-10.

Primary conditionDepressionRegistry: Anxiety DisordersReclassifiedWhy we changed it
Registry
Anxiety Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Depression
Why
  1. The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it.
  2. The study's listed conditions name Depression.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by University of Guadalajara · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 2 years after the study started (first participant enrolled Aug 2024, registered Sep 2026).

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Phase
Not applicable
Study type
Interventional
Enrollment
135
Allocation
Non-randomized
Ages
18 Years to 26 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 65 studies in Depression with a site in Mexico — 10 open to participants now, 11 under way, 2 of them phase 3. Depression · Mexico.

Enrollment
28th of 51
135 · median 159
Started
2024
with 7 others
No phase
24 of 65
5 open now
Registered
65th of 65
by date

Among the 65 studies in Depression with a site in Mexico, this one is the 28th largest by enrollment of the 51 interventional ones that give a count, is one of 8 that started in 2024, is one of 24 with no phase, and was the 65th registered.

Depression

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

Browse Depression studies →

Open to participants now

10 of the 65 studies in Depression with a site in Mexico are open now. Recruiting first, the newest first:

5 more — sign in →

All 10 open studies →

A study can be open while its sites in Mexico have not opened yet or have stopped. Only those recruiting at a site in Mexico →

Who these studies take

Of the 1,089 Depression studies recruiting now, 470 (43%) set no upper age limit and 519 (48%) stop at 75 or younger; 203 take children under 18; 311 take healthy volunteers.

This study: 18 Years to 26 Years · all sexes · no healthy volunteers.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 65 studies in Depression with a site in Mexico, or all of them as a file.
02

Study summary

Objective: To evaluate the association between ACT-process with negative psychological variables in a cross-sectional design, and to evaluate the effect of an ACT-based intervention to diminish anxiety in a sample of medical students.

Methods: An ACT-based intervention was designed to diminish anxiety in medical students and implemented in 4 in-person sessions, the pre-test and post-test measurements were performed one week before and one week after the first and last sessions respectively. The control group received a mental health psychoeducational intervention of 90 minutes. The students were intentionally assigned to each study group based on schedule availability. The cross-sectional study was performed with the pre-test measurements in the students of both groups.\<

Read the detailed description

Here we detail the methodology employed:

PARTICIPANTS AND METHODS Ethics The study was performed according to the Declaration of Helsinki. The protocol was approved by the Research and Ethics Committees of CUCS of the University of Guadalajara with the approval number CI-03023. All participants signed an informed consent form prior to enrollment. The interventions were delivered by health professionals trained in ACT.

Participants Adult medical students at the Health Sciences University Center of the University of Guadalajara who were studying from first to third semesters were invited to participate. The exclusion criteria were a) students that were participating in other psychological of intervention program, and b) students that did not complete all the sessions of the intervention.

Study period: The study was performed in two time points, one in 2023 and the second in 2025, in these two time points the intervention was performed to different participants by different instructors, finally the analyses were conducted with the combined sample.

Measurements Variables: The following variables were measured: psychological flexibility, assessed through four instruments corresponding to ACT-specific processes: the Acceptance and Action Questionnaire-II (AAQ-II) (Espinosa et al., 2010), range 1 - 7, measuring experiential avoidance; the Cognitive Fusion Questionnaire (CFQ) (Ruiz et al., 2017), range 1 - 7, measuring cognitive fusion; the Mindful Attention Awareness Scale (MAAS) (López-Maya, 2015), range 1 - 6, measuring mindfulness, and the Valuing Questionnaire (VQ), (Ruiz et al., 2021), range 0 - 6, measuring consistency with personal values. Negative psychological variables included anxiety, measured with the Generalized Anxiety Disorder scale (GAD-7), range 0 - 3, (Spitzer \& Kroenke, 2006; García-Campallo et al., 2010), depression, measured with the Patient Health Questionnaire-9 (PHQ-9), (Kroenke et al., 2001; Baader et al., 2012), range 0 - 3, somatization, measured with the Patient Health Questionnaire-15 (PHQ-15) (Ros-Montalbán et al., 2010), range 0 - 2, and stress, measured with the Perceived Stress Scale (PSS-14) (Cohen et al., 2010; Remor et al., 2006), range 0 - 4. Sleep satisfaction was assessed with the first item of the Oviedo Sleep Questionnaire (Bobes-García et al., 2000), range 1 to 7.

Sociodemographic and personal variables including age, sex, semester, relationship status (yes, no), socioeconomic level, measured as low, medium and high, alcohol and smoking consumption frequency (from never to 4 or more times in the week), daily minutes of physical activity, daily hours of free time, employment status (yes, no), history of psychological treatment (yes, no), and the number of self-reported health condition (21 different conditions including anxiety, depression, skin diseases, overweight, migraine, colitis, gastritis, allergies, gastrointestinal or respiratory infections, sinusitis, thyroid problems, hypertension, anorexia/bulimia, high cholesterol, renal problems, diabetes, rheumatic conditions, cardiac diseases, cerebral stroke and cancer). The presence of suicide ideation and suicide behavior were measured with the questions: "have you had thoughts of taking your own life?" and "have you taken any actions to try to take your own life?", respectively (answer options, yes, no). All these variables were collected via a Google Forms questionnaire.

Study 1. Design: Study one consisted in a cross-sectional design aimed in determining the correlation among the ACT-related variables with anxiety, depression and stress.

Participants: The participants were those who complied the selection criteria previously described.

Variables: The variables previously described and measured in the pre-test of the intervention program were included for this analysis.

Study 2. Design: This is a cuasi-experimental design with a pre-test and post-test measurements and a control group (psychoeducational session).

Participants: The students were directly invited in their classrooms to either of the 2 interventions in order to facilitate their participation in one schedule, those who accepted to participate were summoned at the University facilities in a schedule convenient for them and the instructor, to receive either the intervention program or the psychoeducational session on mental health.

Procedures: The experimental group received four weekly in-person group sessions based on ACT, conducted at the university facilities. The sessions addressed the six core processes of ACT (acceptance, cognitive defusion, being present, self as context, values, and committed action), with the therapeutic content oriented toward anxiety management. Session duration was 90 to 120 minutes. The sessions program is described in Table 1. The control group received a single psychoeducational session on mental health (90 minutes duration), which included a brief explanation of some techniques for anxiety regulation.

Variables: The previously mentioned variables were measured one week before intervention and 1 week after the final session. Measurements in the control group were conducted at the same time points as those in the intervention group. All measurements were performed via a google form questionnaire.

Table 1. Session program implemented in the intervention group Session number Objective General procedure

  1. - Acceptance To facilitate the development of acceptance regarding unpleasant internal experiences (thoughts, emotions and physical sensations related with anxiety) a) Welcome b) Brief explanation of the specific process of ACT. c) Mindfulness exercise d) Exercise with metaphors related with the specific ACT process. e) Reinforce the process in daily life and give the participants related exercises as homework.
  2. - Defusion and contact with the present moment. To reduce the impact of thoughts in anxiety or psychological distress by developing skills for cognitive defusion, by observing thoughts without becoming entangled in them, and conscious contact with the present moment.
  3. - Me as a context and living values To foster a flexible perspective of the self (self as a context) and clarify personal values as compass for behavior, regardless of the presence of difficult internal experiences.
  4. - Committed action Promote the execution of behaviors aligned with personal values, even in the presence of anxiety or psychological distress, thereby consolidating what was learned in previous sessions.

ACT: Acceptance and commitment therapy. Statistical analysis Descriptive statistics were obtained with means and standard deviations for quantitative variables with parametric distributions and with median and interquartile range for quantitative variables with non-parametric distributions. For qualitative variables frequencies and percentages were obtained. To perform the description of negative psychological variables including anxiety, depression, stress and somatization we obtained 4 to 5 categories (from low to severe) by dividing the possible range of each variable in the number of categories, the categories were determined according to the original instrument recommendations. To evaluate the instrument reliability of all psychological variables, the Cronbach alpha test was performed.

Study 1: Associations between ACT-specific variables, sociodemographic variables, and negative psychological variables were analyzed using Pearson's and Spearman's correlation tests depending on the data distribution. To determine the variables most associated with anxiety we performed a multivariate regression analysis using the stepwise method and including all the studied variables (dichotomous, quantitative and ordinals) as independent variable and excluding suicide ideation, suicide behavior and the negative psychological variables (depression, stress and somatization), this last by considering that these variables would not add information as effective predictors and possible objectives to reduce anxiety.

Study 2: To compare quantitative variables between groups at baseline, the student's t-test or Mann-Whitney U test was applied for parametric and non-parametric distributions, respectively, and the chi-squared test or Fisher's exact test was used for qualitative variables. To evaluate the effect of the intervention, the difference in each variable (posttest minus pretest) was compared between the experimental and control groups using the student's t-test or Mann-Whitney U test. Effect sizes were calculated using Cohen's D test. All analyses were conducted with SPSS software 31 and JASP program (JASP version 0.95.2) (JASP, 2025).

03

Conditions studied

  • Anxiety
  • Somatization
  • Depressive Symptom
  • Stress (Psychology)

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Keywords

  • psychological intervention
04

In context

Depression Reclassified

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

This study's enrollment of 135 is above the median of 81 across 7,066 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

University of Guadalajara is the lead sponsor of 95 studies on the registry; 18 are open to participants now.

Compared within Depression, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →

05

Who can participate

Ages eligible
18 Years to 26 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult medical students at the Health Sciences University Center of the University of Guadalajara
  • who were studying from first to third semesters were invited to participate.

Exclusion criteria

Exclusion Criteria:

  1. students that were participating in other psychological of intervention program
  2. students that did not complete all the sessions of the intervention.
06

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
135 participants (actual)

Study arms

  • Experimental
    ACT_based intervention

    This arm was assigned to the ACT\_based therapy, which consisted in 4 weekly sessions of 2 hours, including information about: : Session number Objective General procedure 1.- Acceptance To facilitate the development of acceptance regarding unpleasant internal experiences (thoughts, emotions and physical sensations related with anxiety) 2.- Defusion and contact with the present moment. To reduce the impact of thoughts in anxiety or psychological distress by developing skills for cognitive defusion, by observing thoughts without becoming entangled in them, and conscious contact with the present moment. 3.- Me as a context and living values To foster a flexible perspective of the self (self as a context) and clarify personal values as compass for behavior, regardless of the presence of difficult internal experiences 4.- Committed action: promote execution of behaviors aligned with personal values

    Behavioral: ACT_based intervention

  • Active comparator
    Active control group

    This group was assigned to an active computation group which consisted in a single psychoeducational 90 minutes session about mental health, which included the explanation of techniques to diminish anxiety

    Behavioral: Active Control group

Interventions

  • BehavioralACT_based intervention

    Session number Objective General procedure 1. \- Acceptance To facilitate the development of acceptance regarding unpleasant internal experiences (thoughts, emotions and physical sensations related with anxiety) 2. \- Defusion and contact with the present moment. To reduce the impact of thoughts in anxiety or psychological distress by developing skills for cognitive defusion, by observing thoughts without becoming entangled in them, and conscious contact with the present moment. 3. \- Me as a context and living values To foster a flexible perspective of the self (self as a context) and clarify personal values as compass for behavior, regardless of the presence of difficult internal experiences 4. \- Committed action: promote execution of behaviors aligned with personal values

  • BehavioralActive Control group

    This group received a 90-minutes psychoeducational session about mental health including a brief explanation of what anxiety is, its risk factors and symptoms and techniques for anxiety regulation including the psychological interventions as Behavioral therapy, acceptance and commitment therapy and mindfulness, and the description of conductual changes that can reduce anxiety.

07

What researchers measure

Primary outcomes

  1. Anxiety symptos

    This measure was performed with the General Anxiety Disease (GAD-7) questionnaire.

    Time frame: From enrollment to the end of the study after 4 weeks

08

Study locations

1 site
  • University of Guadalajara, Health Sciences University Center
    Guadalajara, Jalisco 44340, Mexico
09

References and documents

Individual participant data

Plan to share: No — We do not plan to share IPD, as the according to the local ethics committee, we are not allowed to share this information being considered confidential

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2024 to primary completion in Dec 2025, 16 months.

Of 3,471 non-industry interventional studies with no phase under Depression, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's 16 months is below that.

Counting every sponsor, half of 3,569 studies reached it within 21 months; a quarter within 9 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 4, 2026
First posted
Sep 10, 2026
StartActual
Aug 5, 2024
Primary completionActual
Dec 14, 2025
CompletionActual
Dec 14, 2025
Last update
Sep 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT07813520
Lead sponsor
University of Guadalajara
Responsible party
Aniel Jessica Leticia Brambila-Tapia (Profesora e Investigadora Titular A, University of Guadalajara) — Principal investigator
First posted
Sep 10, 2026
Start date
Aug 5, 2024
Primary completion
Dec 14, 2025
Completion
Dec 14, 2025
Last update
Sep 10, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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