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Patient Comfort During Dermatologic Procedures

Managing Patient Comfort During Dermatologic Procedures: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02816996
Enrollment
135
Registered
2016-06-29
Start date
2017-01-24
Completion date
2017-04-26
Last updated
2021-12-06

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

Conditions

Anxiety, Pain

Brief summary

The goal of this study is to find the effect of holding a patient's hand on anxiety and pain during dermatologic procedures.

Interventions

PROCEDUREHand-holding

Subject will have their hand held.

PROCEDUREStress Ball

Subject will be given a stress ball to hold.

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Age 18 and older * Undergoing a dermatologic procedure * Willing and able to understand and provide informed consent and communicate with the investigator

Exclusion criteria

* Subjects who have wound healing problems * Subjects who are unable to understand the protocol or to give informed consent * Subjects with self-reported mental illness or other psychological conditions, such as psychotic disorders, mood disorders, anxiety disorders, cognitive disorders, depression with psychotic features, dissociative disorders

Design outcomes

Primary

MeasureTime frameDescription
Anxietyimmediately after dermatologic procedureSubjects will complete the 6-item State-Trait Anxiety Inventory (STAI)
Painimmediately after dermatologic procedureSubjects will complete a visual analog scale for pain ranging from no pain at all to worst possible pain.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026