Skip to content

My Mindful Moments: A Mindfulness Meditation and Digital Art Activity

My Mindful Moments: A Mindfulness Meditation and Digital Art Activity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04557033
Enrollment
16
Registered
2020-09-21
Start date
2021-07-01
Completion date
2022-07-30
Last updated
2022-08-25

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

Conditions

Meditation, Mindfulness

Keywords

Mindfulness, Meditation

Brief summary

The purpose of this evidence-based practice project is to evaluate the feasibility of providing a relaxation mindfulness meditation and an expressive digital arts activity among clinical staff at Dana Farber Cancer Institute .

Detailed description

This project provides an opportunity for patient care staff in an ambulatory oncology setting to participate in and evaluate an activity that includes a mindfulness meditation technique and an expressive digital arts activity. This study will be conducted to evaluate the feasibility of providing a mindfulness meditation and digital imagery activity. * The activity will include a guided mindfulness meditation and the creation of a digital image on an iPad. * Participants will be asked to complete brief surveys before and after the intervention activity.

Interventions

OTHERMindfulness intervention

My Moments® application (app) is a tool used to facilitate expressive art creation in a digital photography media

Sponsors

Dana-Farber Cancer Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults ≥18 years of age * Currently employed at Dana Farber Cancer Institute * Providing patient care on Yawkey

Exclusion criteria

* Not an employee of Dana Farber Cancer Institute * Not providing Patient Care on Yawkey

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participation-Feasibility1 year≥50% of staff choose to participate=Feasibility. This measure of feasibility will be evaluated by calculating index scores of the percentage of clinical staff who choose to participate
Percentage Completion of Full Activity-Feasibility1 year\> 80% of those who participate complete the activity=Feasibility. This measure of feasibility will be evaluated by index scores of the percentage of clinical staff who complete the full activity
Mean Completion Time-Feasibility1 yearThe activity is completed by the group in 40 minutes or less-Feasibility. This measure of feasibility will be evaluatedby individual group completions times and overall analysis of descriptive statistics on the time for completion of the activity by all groups.

Secondary

MeasureTime frameDescription
Change in Anxiety Score1 YearChanges in participant state anxiety will be evaluated using the visual analogue scale in measuring state anxiety. The electronic scale displays a horizontal line divided into 30 equal-sized partitions. The left edge of the scale is marked calm and the right edge is marked anxious. A sliding locator is positioned at the midpoint of the scale. The participant is instructed to use the computer mouse to place the locator at the scale position representing their current level of anxiety. The score is automatically calculated by rounding the relative distance of the locator from the left edge of the scale to the nearest integer value between 0 and 30. A higher score indicates greater anxiety. A comparison of scores pre- and post- intervention by calculating a paired t-test comparison of means

Countries

United States

Outcome results

None listed

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