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Mindfulness in Endometrial and Cervical Cancer

Mindfulness Practice in Endometrial and Cervical Cancers With Smartphone Applications (MECCA)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04512144
Acronym
MECCA
Enrollment
120
Registered
2020-08-13
Start date
2020-07-25
Completion date
2026-07-30
Last updated
2025-09-30

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

Conditions

Cervical Cancer, Endometrial Cancer, Gynecologic Cancer, Opioid Use, Quality of Life

Brief summary

Patients with endometrial cancer who will be undergoing surgery or patients with cervical cancer who will be treated with chemoradiation will be randomized to utilize the Headspace smartphone application or not prior to their anticipated treatment.

Detailed description

A diagnosis of cancer can be a major stress-inducing event. The prevalence of depression in patients diagnosed with cancer is estimated up to 16%. Practicing mindfulness is a cost-effective treatment which can also help manage treatment adverse effects and cancer-related symptoms. Even short exposure and practice of mindfulness exercises have demonstrated improved subjective and objective measurements of stress and anxiety with breast biopsies. Patients with breast cancer also have improved quality of life with mindfulness training. Self-guided mindfulness with smartphone applications, specifically the app Headspace, has been associated with positive benefits and ease of use in the general population and among cancer patients. A patient's inherent level of baseline mindfulness has been associated with lower pain scores following minimally invasive hysterectomy. This study did not specifically encourage practice of mindfulness exercises. Our own study of post-operative opiate usage in women following minimally invasive hysterectomy contains self-reported data of women using opiates to relax or help sleep. This suggests that mindfulness exercises may improve quality of life in these areas and thus reduce opiate usage. Patients undergoing minimally invasive hysterectomy for treatment of endometrial cancer were specifically chosen as a study cohort to build on our own data and that currently reported in the literature as well as the highest incidence of this cancer as a gynecologic malignancy. The second study cohort chosen was women with cervical cancer undergoing definitive treatment with chemo-sensitizing radiation given the significant endeavor required for complete treatment. Additionally, these women are often younger with the diagnosis of cervical cancer often being their first major medical diagnosis.

Interventions

BEHAVIORALHeadspace Smartphone Application

Headspace is a smartphone application used for mindfulness, meditation, and stress reduction. It has been utilized in other behavioral and quality of life studies.

Sponsors

St. Louis University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* New diagnosis of either 1) endometrial cancer undergoing surgery or 2) cervical cancer undergoing chemo-sensitizing radiation * Access to a smartphone

Exclusion criteria

* Non-English speaking * No access to smartphone * Current use of Headspace application

Design outcomes

Primary

MeasureTime frameDescription
Opiate Usage-Endometrial cancerEnrollment to 30 days post op for endometrial cancer.The amount of opiates used during the acute (30 day) recovery after surgery for endometrial cancer or acute treatment with chemoradiation for cervical cancer will be recorded.
Opiate Usage-Cervical CancerEnrollment to 6 weeks post treatment for cervical cancer.The amount of opiates used during the acute treatment with chemoradiation for cervical cancer will be recorded.

Secondary

MeasureTime frameDescription
Complication RatesEnrollment to 4 weeks post op for endometrial cancer. Enrollment to 6 weeks post treatment for cervical cancer.Surgical or treatment complications will be monitored in each group.
Five Facet Mindfulness QuestionnaireEnrollment to 4 weeks post op for endometrial cancer. Enrollment to 6 weeks post treatment for cervical cancer.Patients will be asked to complete a Five Facet Mindfulness Questionnaire form at enrollment, on the day of surgery (endometrial cancer) or first brachytherapy (cervical cancer), and at their post-treatment visit.
ComplianceEnrollment to 4 weeks post op for endometrial cancer. Enrollment to 6 weeks post treatment for cervical cancer.The number of Headspace sessions utilized by patients in the intervention group will be recorded.
Patient satisfactionEnrollment to 4 weeks post op for endometrial cancer. Enrollment to 6 weeks post treatment for cervical cancer.Patients from each group will be asked to complete an anonymous study-specific survey evaluating their satisfaction with the program.
Functional Assessment of Cancer Therapy-GeneralEnrollment to 4 weeks post op for endometrial cancer. Enrollment to 6 weeks post treatment for cervical cancer.Patients will be asked to complete a Functional Assessment of Cancer Therapy-General form at enrollment, on the day of surgery (endometrial cancer) or first brachytherapy (cervical cancer), and at their post-treatment visit.

Countries

United States

Contacts

Primary ContactShannon Grabosch, MD
shannon.grabosch@health.slu.edu3147818605
Backup ContactShohreh Jamalabadi-Majidi, DMD, MPH
shohreh.jamalabadimajidi@health.slu.edu3149777482

Outcome results

None listed

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