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The Effectiveness of Three Good Things on Gratitude and Psychological Well-being Among Nursing Students

NCT07337200 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 277

Last updated 2026-01-13

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if the daily Three Good Thing intervention can prevent negative mental health outcomes like stress and burnou, and promote Gratitude and Psychological Wellbeing in undergraduate Nursing Students.

The main questions it aims to answer are:

Does the daily Three Good Things intervention effective in promoting gratitude and psychological wellbeing among nursing students?

Researchers will compare four different arms from Solomon Four Group Design to see if the increase in Gratitude and Psychological Wellbeing scores is significantly greater in the groups that received the 3GT intervention.

Participants will be randomly assigned to one of the four groups, and those in the intervention groups will:

1. Complete a pre-test questionnaire (for some groups) on their current level of Gratitude and Psychological Wellbeing.
2. Perform the Three Good Things (3GT) intervention by writing down three positive things that happened each day for 7 consecutive days.
3. Complete a post-test questionnaire to measure the final level of Gratitude and Psychological Wellbeing.

Conditions

  • Nursing Student
  • Gratitude
  • Psychological Well-being

Interventions

BEHAVIORAL

Three Good Things

The Three Good Things intervention was self-administered daily for seven days. Participants are required to record three positive things that happened that day and add a brief summary of the reasons behind these events using a Google form prepared by the researchers.

Sponsors & Collaborators

  • Kaohsiung Medical University

    lead OTHER

Principal Investigators

  • Yudisa Diaz Lutfi Sandi RN, MSN, RN., PhD · School of Health Science, Politeknik Negeri Subang

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-12-23
Primary Completion
2026-03-01
Completion
2026-03-25

Countries

  • Indonesia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07337200 on ClinicalTrials.gov