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Not yet recruitingNCT07085897Updated Jul 25, 2025

Web-based Single-session Growth Mindset Intervention for Allied Health Practicum Trainees to Reduce Anxiety

An interventional study of Web-based Single-session Intervention of Mindset on Intelligence, Failure, and Emotion (We-SMILE) for allied health practicum trainees in Anxiety, sponsored by The Hong Kong Polytechnic University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-07-25.

Sponsored by The Hong Kong Polytechnic University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Jan 2026, 8 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Practicum is a critical component of professional training, offering essential experiential learning opportunities that support the development of future practitioners. However, existing research indicates that practicum can be particularly challenging for allied health students, who must navigate both academic learning adjustments and complex healthcare environments. Emerging evidence also highlights the potential value of low-intensity, self-guided interventions in enhancing practicum trainees' psychological preparedness. Based on the findings, this present project adapts an integrated intervention-the Web-based Single-Session Intervention on Mindset regarding Intelligence, Failure, and Emotion (We-SMILE)-specifically for practicum students in allied health professions and examines its efficacy to adjust their mindsets and manage practicum-related challenges more effectively.

Using a two-arm randomised controlled trial, the proposed study will examine the efficacy of We-SMILE for allied health practicum trainees in reducing anxiety, as well as improving perceived stress, performance anxiety, practicum-related concerns, psychological status, learning orientation, confidence, resilient coping, and time management.

Students commencing their practicums will be recruited from allied health programmes and randomly assigned to either existing pre-practicum training plus intervention or the training-as-usual control group. Participants will be assessed at three time-points: baseline before intervention (T1), two weeks post-intervention (T2) and two months post-intervention (T3). The intention-to-treat principle and linear-regression-based maximum likelihood multi-level models will be used for data analysis.

Feasibility and Potential: This project brings together experts in mindset research, fieldwork coordinators, and programme leaders, ensuring the feasibility of the study. It will not only generate evidence on the adapted We-SMILE intervention for allied health practicum trainees but also offer a scalable and accessible model for enhancing the well-being of trainees in other healthcare and helping professions.

02

Conditions studied

  • Anxiety

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03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's planned enrollment of 120 is above the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

The Hong Kong Polytechnic University is the lead sponsor of 659 studies on the registry; 250 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
No

Inclusion criteria

  • Students enrolled in allied health programmes who are about to commence their practicums or have recently entered practicum.

Exclusion criteria

Exclusion Criteria:

  • (1) do not consent to participate, (2) cannot concentrate for at least 45 minutes to complete the intervention and questionnaires, (3) have a disability or serious physical or mental illness resulting in poor condition, and (4) do not participate in the practicum.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Web-based Single-session Intervention of Mindset on Intelligence, Failure, and Emotion (We-SMILE)

    The intervention is structured into three video-and-exercise sessions. Part one focuses on students' mindsets in coping with practicum-related challenges and their attitudes towards setbacks, encouraging them to shift from a 'fear-of-failure' mindset to a 'failure-is-enhancing' mindset. Part two introduces the nature and concept of neuroplasticity to promote students' understanding of effective learning. Part three centers on providing guidance for students on strategies to cope with stress and emotional turbulence with growth mindset regarding emotion.

    Behavioral: Web-based Single-session Intervention of Mindset on Intelligence, Failure, and Emotion (We-SMILE) for allied health practicum trainees

  • No intervention
    Training-as-usual group

    The training-as-usual group will continue the regular practicum training.

Interventions

  • BehavioralWeb-based Single-session Intervention of Mindset on Intelligence, Failure, and Emotion (We-SMILE) for allied health practicum trainees

    The intervention is structured into three video-and-exercise sessions. Part one focuses on students' mindsets in coping with practicum-related challenges and their attitudes towards setbacks, encouraging them to shift from a 'fear-of-failure' mindset to a 'failure-is-enhancing' mindset. Part two introduces the nature and concept of neuroplasticity to promote students' understanding of effective learning. Part three centers on providing guidance for students on strategies to cope with stress and emotional turbulence with growth mindset regarding emotion.

06

What researchers measure

Primary outcomes

  1. Anxiety related to practicum

    Anxiety related to practicum will be measured by four items, including "level of anxiety about starting the practicum", "how much your anxiety will interfere with their learning", "how prepared you are for the practicum" and "how excited you are to participate in the practicum". Each statement will be rated on a 10-point Likert scale, ranging from 1=completely not anxious, very small, completely unprepared, and completely unexcited to 10=extremely anxious, very great, perfectly prepared, and extremely excited.

    Time frame: Baseline, 2-week and 8-week follow-ups

Secondary outcomes

  1. Psychological states

    Psychological states will be assessed by the Depression, Anxiety and Stress Scale-8 Items (DASS-8) is a set of three self-report scales designed to measure the psychological states of depression, anxiety and stress. Each of the depression and anxiety sub-scales of the DASS-8 contain 3 items while the stress sub-scale contains 2 items. Each item can be scored from 0 (Did not apply to me at all) to 3 (Applied to me very much, or most of the time).

    Time frame: Baseline, 2-week and 8-week follow-ups

  2. Performance anxiety

    Performance anxiety will be examined by the sub-scale of cognitive anxiety from the Performance Test Anxiety questionnaire (PTA). Respondents indicated how they were thinking and feeling about their practicum (using a 5-point scale on which 1=totally disagree and 5=totally agree) in response to the items.

    Time frame: Baseline, 2-week and 8-week follow-ups

  3. Learning orientation

    Learning orientation will be assessed by five items (e.g., "I like to learn new knowledge in practicums."). Each item will be rated by a five-point Likert scale from 1=strongly disagree to 5=strongly agree.

    Time frame: Baseline, 2-week and 8-week follow-ups

  4. Confidence

    Confidence will be assessed by a six-item self-developed scale. Items generated from interviews with practicum students, such as "I am confident that I can listen to comments from supervisors/colleagues/service users with an open mind." and "I am confident that I can manage my time well and cope with my practicum work and schoolwork at the same time.". Each item needs to be rated from 1=strongly disagree to 5=strongly agree.

    Time frame: Baseline, 2-week and 8-week follow-ups

  5. Resilient Coping

    Resilient Coping will be measured by a self-report four-item Brief Resilient Coping Scale (BRCS). Items will be scored from 1 (Does not describe me at all) to 5 (Describe me very well). A sample item is "I look for creative ways to alter difficult situations".

    Time frame: Baseline, 2-week and 8-week follow-ups

  6. Perceived stress

    Stress will be examined by the Perceived Stress Scale-4 items (PSS-4). It measures the degree to which situations in one's life over the past month are appraised as stressful. Each item will be scored from 0 (Never) to 4 (Very often). Total score is determined by adding together the scores of each of the four items. Questions 2 and 3 are reverse coded.

    Time frame: Baseline, 2-week and 8-week follow-ups

  7. Practicum-related concerns

    Practicum-related concerns will be assessed using a self-developed six-item scale designed to reflect the concerns of allied health students.

    Time frame: Baseline, 2-week and 8-week follow-ups

  8. Time management

    Time management will be assessed using the 'Setting Goals and Priorities' sub scale of the Time Management Behavior (TMB) Scale, which includes ten items. Each item is rated on a 5-point Likert scale ranging from 1 (seldom true) to 5 (very often true).

    Time frame: Baseline, 2-week and 8-week follow-ups

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07085897
Lead sponsor
The Hong Kong Polytechnic University
Responsible party
Sponsor
First posted
Jul 25, 2025
Start date
Aug 10, 2025 (estimated)
Primary completion
Jan 31, 2026 (estimated)
Completion
Mar 31, 2026 (estimated)
Last update
Jul 25, 2025

Study contacts

Shimin Zhu, PhD
Contact
jasmine.zhu@polyu.edu.hk
+852 2766 5787

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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