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CompletedNCT07699835Updated Jul 13, 2026

Efficacy of a Gamified Blended Mindfulness Program to Reduce Burnout, Stress, and Anxiety in Nursing Students: A Randomized Controlled Trial

An interventional study of Psychoeducation and Free App Recommendation and Standard Blended Mindfulness Program in Burnout Syndrome, Psychological Stress, Anxiety, and Depression Associated With Academic Pressure and Anxiety, sponsored by Universidad de Granada. Completed at 1 site in Spain. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-13.

Sponsored by Universidad de Granada · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 1 year 5 months after the study started (first participant enrolled Feb 2025, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
127
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The primary purpose of this randomized controlled trial is to evaluate the efficacy of a 12-week gamified blended mindfulness intervention in reducing academic burnout, perceived stress, and anxiety among first-year nursing students. Nursing students frequently face high academic and clinical demands that deplete their psychological resources, leading to high levels of stress and emotional exhaustion during their training. While mindfulness interventions can mitigate these negative effects, adherence to standard digital programs often remains a challenge.

To address this, the study investigates the impact of incorporating gamification elements into a mindfulness program. Participants are randomly assigned to one of three groups: a minimal-treatment control group, a standard blended mindfulness group, or a gamified blended mindfulness group. The intervention spans 12 weeks and consists of 24 guided meditation sessions (16 online and 8 in-person).

The central hypothesis is that the gamified architecture will act as a behavioral reinforcement mechanism, improving student adherence to the program. Consequently, researchers hypothesize that participants in the gamified group will exhibit significantly lower post-intervention levels of emotional exhaustion, perceived stress, and anxiety compared to those in both the standard mindfulness intervention and the control group.

02

Conditions studied

  • Burnout Syndrome
  • Psychological Stress, Anxiety, and Depression Associated With Academic Pressure
  • Anxiety

Keywords

  • Mental Health Promotion
  • Nursing Students
03

In context

Burnout, Psychological

442 studies on the registry are indexed under Burnout, Psychological; 106 are open to participants now.

This study's enrollment of 127 is above the median of 80 across 319 interventional studies indexed under Burnout, Psychological.

Browse Burnout, Psychological studies →

Lead sponsor

Universidad de Granada is the lead sponsor of 241 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Enrolled as a first-year undergraduate nursing student at the Ceuta Campus of the University of Granada (Spain).
  • Aged 18 years or older.
  • Voluntarily provide informed consent prior to participation.

Exclusion criteria

Exclusion Criteria:

  • Pre-existing clinical diagnosis of anxiety or depressive disorders.
  • Current use of prescribed psychotropic medications (concurrent psychopharmacological treatment).
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
127 participants (actual)

Study arms

  • Active comparator
    Control Group

    Participants in this control cohort (CG) receive a single-session minimal psychoeducational intervention rather than a structured multi-week mindfulness program.

    Behavioral: Psychoeducation and Free App Recommendation

  • Active comparator
    Intervention Group 1

    Participants in this group (IG1) receive a structured 12-week blended mindfulness-based stress-reduction program without any gamification elements.

    Behavioral: Standard Blended Mindfulness Program

  • Experimental
    Intervention Group 2

    articipants in this group (IG2) receive the standard 12-week blended mindfulness program enhanced with a structured gamified architecture designed to increase adherence and engagement.

    Behavioral: Gamified Blended Mindfulness Program

Interventions

  • BehavioralPsychoeducation and Free App Recommendation

    Participants receive baseline information regarding the definition and health effects of meditation, alongside advice on how to independently practice it using free sessions available on a mobile application.

  • BehavioralStandard Blended Mindfulness Program

    A 12-week program consisting of 24 guided meditation sessions (16 online and 8 in-person). Sessions are led by a mindfulness expert, last between 15 and 30 minutes, and focus on breathing techniques and guided meditation practices.

  • BehavioralGamified Blended Mindfulness Program

    A 12-week, 24-session blended mindfulness program (15-30 minutes per session) integrated with gamification elements. Participants earn one point per completed session to enter a draw for a premium nursing training app subscription. The system also provides weekly automated score updates and a final anonymized leaderboard.

06

What researchers measure

Primary outcomes

  1. Academic Burnout: Emotional Exhaustion

    Assessed using the Emotional Exhaustion subscale of the Maslach Burnout Inventory-Student Survey (MBI-SS). This subscale consists of 5 items rated on a 7-point frequency scale ranging from 0 (never) to 6 (daily). Higher scores indicate higher levels of emotional exhaustion.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

Secondary outcomes

  1. Academic Burnout: Cynicism

    Assessed using the Cynicism subscale of the Maslach Burnout Inventory-Student Survey (MBI-SS). It consists of 4 items rated on a 7-point scale (0 = never to 6 = daily). Higher scores indicate higher levels of cynicism toward studies.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  2. Academic Burnout: Academic Efficacy

    ssessed using the Academic Efficacy subscale of the Maslach Burnout Inventory-Student Survey (MBI-SS). It consists of 6 items rated on a 7-point scale (0 = never to 6 = daily). Higher scores indicate higher levels of academic efficacy (considered a protective factor against burnout).

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  3. Perceived Stress

    Assessed using the 10-item Perceived Stress Scale (PSS). Higher total scores indicate higher levels of perceived stress.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  4. Anxiety

    Assessed using the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS). This subscale consists of 7 items, each scored from 0 to 3, with subscale totals ranging from 0 to 21. Higher scores indicate higher levels of anxiety symptomatology.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  5. Depression

    Assessed using the depression subscale of the Hospital Anxiety and Depression Scale (HADS). This subscale consists of 7 items, each scored from 0 to 3, with subscale totals ranging from 0 to 21. Higher scores indicate higher levels of depressive symptomatology.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  6. Student Engagement

    Evaluated using the 9-item short version of the Utrecht Work Engagement Scale for Students (UWES-9). All items use a 0-6 frequency scale. Higher scores indicate higher levels of academic work engagement.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

  7. Dispositional Mindfulness

    Measured by the Mindful Attention Awareness Scale (MAAS). This is a 15-item instrument designed to assess core characteristics of dispositional mindfulness, specifically open awareness and attention to the present moment. Higher scores denote greater mindfulness.

    Time frame: Baseline (T0) and immediately following the 12-week intervention period (T1).

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Study locations

1 site
  • Ceuta
    Ceuta, Ceuta 51005, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07699835
Lead sponsor
Universidad de Granada
Responsible party
María José Membrive Jiménez (Professor, Universidad de Granada) — Principal investigator
First posted
Jul 13, 2026
Start date
Feb 1, 2025
Primary completion
Sep 5, 2025
Completion
Mar 1, 2026
Last update
Jul 13, 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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