Skip to content

Effect of the Subconscious on Mohs Micrographic Surgery

Effect of the Subconscious on Mohs Micrographic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00374062
Enrollment
150
Registered
2006-09-08
Start date
2007-12-31
Completion date
2009-08-31
Last updated
2014-07-15

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

Conditions

Basal Cell Carcinoma, Squamous Cell Carcinoma

Keywords

Mohs Surgery

Brief summary

The goal of this study is to determine if relaxation therapy improves patient satisfaction with Mohs micrographic surgery.

Detailed description

Patients are instructed in relaxation techniques. The goal of this study is to determine how relaxation techniques affect the patient's Mohs micrographic surgery experience.

Interventions

BEHAVIORALrelaxation therapy 1

relaxation therapy 1

BEHAVIORALrelaxation therapy 2

relaxation therapy 2

BEHAVIORALrelaxation therapy 3

relaxation therapy 3

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Age 25 and older * Subjects are undergoing micrographic Mohs surgery for facial basal and squamous cell carcinoma. * The subjects are in good health. * The subjects have willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator.

Exclusion criteria

* Subjects who have wound healing problems. * Subjects who have had prior Mohs surgery. * Subjects who are smokers. * Subjects who are currently using anticoagulation therapy * Subjects who have a history of bleeding disorders. * Subjects who are unable to understand the protocol or to give informed consent * Subjects with known mental illness or other psychological conditions, such as psychotic disorders, mood disorders, anxiety disorders, cognitive disorders, depression with psychotic features, dissociative disorders. * Subjects who are taking medications that may affect healing such as prednisone, or any immunosuppressants. * Subjects who are immunocompromised. * Subjects who have Diabetes Mellitus or any other condition determined by the PI to affect healing.

Design outcomes

Primary

MeasureTime frame
Patient anxiety1 day

Secondary

MeasureTime frame
Scar appearance12 weeks

Countries

United States

Outcome results

None listed

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