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Mindful Coloring to Reduce Nurses' Stress

Coloring as a Brief Mindfulness-based Intervention for Stress Reduction Among Nurses

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04942509
Enrollment
79
Registered
2021-06-28
Start date
2020-12-07
Completion date
2021-01-12
Last updated
2021-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn Out (Psychology), Stress (Psychology)

Keywords

nurses, coloring, brief mindfulness-based intervention, mental well-being, mindfulness

Brief summary

The purpose of this study was to investigate whether nurses who did mindful coloring for at least five working days during a 10-day period experienced stress reduction afterwards.

Detailed description

Enrolled participants who met inclusion criteria (full-time clinical nurses working for at least five days during a specified 10-day period) were randomized in 1:1 ratio to the coloring or control groups. A third party did the allocation sequence and concealment. After giving informed consent, participants completed the baseline questionnaire and the coloring group watched an instructional video on mindful coloring. The coloring group were asked to color for any length of time on at least five working days during a 10-day period (period A) while the control group were asked to do it on a subsequent 10-day (period B). The post-intervention questionnaire was completed by both groups at the end of period A. The study was completed after period B.

Interventions

BEHAVIORALColoring as a brief mindfulness-based intervention

Participants watched an instructional video on mindful coloring at the beginning of the intervention and colored mindfully for at least 5 days or 100 minutes in total during a 10-day period. The intervention included a coloring booklet that contained mandala patterns for coloring.

Sponsors

City University of Hong Kong
CollaboratorOTHER
Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants were allocated into the experimental and wait-list control groups. The experimental group colored for at least 5 days during a 10-day period while the control group did not.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Full time clinical nurses working under the Hospital Authority who would be working for at least 5 days during a specified 10-day study period.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Change in perceived stressTime point 1: pre-intervention. Time point 2: post-intervention (10 days)Scores of 0-40 measured by the Perceived Stress Scale. A positive outcome is indicated by a lower post-intervention score.

Secondary

MeasureTime frameDescription
Change in mental well-beingTime point 1: pre-intervention. Time point 2: post-intervention (10 days)Scores of 7-35 measured by the short Warwick-Edinburgh Mental Well-being Scale. A positive outcome is indicated by a higher post-intervention score.
Change in burnoutTime point 1: pre-intervention. Time point 2: post-intervention (10 days)Three subscales (each with a separate score) assessing three facets of burnout including Emotional Exhaustion (scores 0-54), Depersonalisation (scores 0-30) and Personal Accomplishment (scores 0-48) measured by the Maslach Burnout Inventory - Human Services Survey for medical personnel. Burnout is represented by a combination of high emotional exhaustion and depersonalization scores, together with a low personal accomplishment score. Positive outcomes are indicated by a lower score in Emotional Exhaustion and Depersonalisation, and a higher score in Personal Accomplishment.
Change in trait mindfulnessTime point 1: pre-intervention. Time point 2: post-intervention (10 days)Scores of 24-120 measured by the Five Facets Mindfulness Questionnaire - short form. A positive outcome is indicated by a higher post-intervention score.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026