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Psychological DistressNCT07910032

Group Psychological Intervention to Reduce Distress Among Nursing Undergraduates

A study testing Intervention program for psychological distress among nursing undergraduates and Routine mental health education in people with Psychological Distress, run by Liu Jingying.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

This is a randomized controlled trial. The study aims to explore the effect of group psychological intervention on academic distress among nursing undergraduates whose score on the self-developed Nursing Undergraduate Academic Distress Scale is ≥29. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Psychological Distress
What is being tested?
Intervention program for psychological distress among nursing undergraduates and Routine mental health education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
84 participants
Where
No sites listed yet
Study dates
1 Nov 2026to Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Full-time undergraduate nursing students;
  • Achieved a score ≥29 on the self-developed Nursing Undergraduate Academic Distress Scale;
  • Aged 18 years or above;
  • Voluntarily participate in this study and signed written informed consent;
  • Able to attend all 8-week group sessions and complete baseline and post-intervention assessments.

Who cannot join

  • Diagnosed with mental disorders or receiving ongoing psychiatric treatment / psychological counseling;
  • Participating in other similar psychological intervention programs at the same time;
  • Unable to persist in the whole 8-week intervention and follow-up assessment due to personal reasons.

About this study

Official title: A Randomized Controlled Trial of Group Psychological Intervention to Reduce Distress Among Nursing Undergraduates

This is a randomized controlled trial. The study aims to explore the effect of group psychological intervention on academic distress among nursing undergraduates whose score on the self-developed Nursing Undergraduate Academic Distress Scale is ≥29. Eligible students will be randomly assigned to the intervention group or the control group. The intervention group will receive an 8-week structured group psychological intervention, while the control group will receive routine mental health education. The primary outcome is the change in academic distress score from baseline to the end of the 8-week intervention. Feasibility of the intervention program will also be evaluated.

Being tested
Intervention program for psychological distress among nursing undergraduates, Routine mental health education

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intervention program for psychological distress among nursing undergraduatesBehavioural

    8-week standardized group intervention program for alleviating psychological distress among nursing undergraduates.

  • Routine mental health educationBehavioural

    General mental health science popularization education.

Study groups in NCT07910032
Study groupRoleWhat they receive
Group psychological interventionExperimentalParticipants will receive an 8-week structured group psychological intervention to alleviate psychological distress.
Receives: Behavioral: Intervention program for psychological distress among nursing undergraduates
Routine mental health educationActive comparatorParticipants will receive routine general mental health education without the targeted distress intervention.
Receives: Behavioral: Routine mental health education

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in psychological distress score

    The change score of psychological distress scale from baseline to post-intervention, which is used to compare the difference of psychological distress level between intervention group and control group.

    Measured: Baseline, immediately after the 8-week intervention, and 1-month follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Nov 2026
  2. Study start1 Nov 2026 (estimated)
  3. Primary completion23 Feb 2027 (estimated)
  4. Study completionApr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
84 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07910032
Sponsor's protocol ID
CMU-2026-Trial-01
Status last verified
Oct 2026
First submitted
27 Oct 2026
Last updated
3 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Intervention program for psychological distress among nursing undergraduates and Routine mental health education in people with Psychological Distress, run by Liu Jingying.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 3 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in psychological distress score (time frame: Baseline, immediately after the 8-week intervention, and 1-month follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Nov 2026.

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