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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03481127
Other study ID # 201711117
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date May 8, 2018
Est. completion date March 26, 2019

Study information

Verified date May 2019
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to understand the feasibility and impact of integrated psychological care in outpatient gynecologic oncology clinics with the goal of creating a new standard of care. The investigators propose an intervention study comparing patient-centered outcomes (assessed by surveys) between women who receive usual care versus integrated psychological care. The investigators' objectives are to learn about the process of integration of psychological care directly into outpatient gynecologic oncology clinics and the impact of such integration on patients' well-being, presentation of symptoms, psychological functioning, coping mechanisms, awareness of support services offered, and perception of quality of care. As this is a feasibility study, aims are focused on assessing patient willingness for psychological intervention in the medical office, provider willingness to have psychologist present in clinic, and impact of psychological intervention. With such data to warrant further integration and time of psychologists in medical clinics, next steps for immediate and long-term projects may include focus on high risk populations, specific disease sites, additional provider clinics, more psychologist time spent in gynecological oncology clinics, and effectiveness of interventions with higher power. The investigators hope the results will serve as preliminary data for an integrated psychosocial care model that can be implemented in other oncology clinics.


Recruitment information / eligibility

Status Completed
Enrollment 101
Est. completion date March 26, 2019
Est. primary completion date August 29, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Aged 18 years or older

- Scheduled for an appointment in a gynecologic oncology clinic at the Siteman Cancer Center at the Center for Advanced Medicine or the Women's Tumor Clinic at the Center for Outpatient Health at Barnes-Jewish Hospital

- Patients may or may not have a cancer diagnosis.

- All gynecologic cancer types, histologic grades, primary or recurrent disease.

- Patients actively undergoing treatment or close observation

- Pregnant or lactating patients

- Able to speak and read English

- Able to consent

Inclusion criteria (correlative studies only) -Patients who are undergoing pre-operative work-up for evaluation of an adnexal mass by a Washington University gynecologic oncologist.

Exclusion Criteria:

-Impaired by a psychiatric or cognitive disorder that limits their ability to give consent or communicate with their medical providers about symptoms (as determined by the patient's medical team)

Exclusion criteria (correlative studies only)

- Neoadjuvant chemotherapy

- Treatment within the past month with antidepressant medications that affect serotonin physiology

- Specific histology: low malignant potential tumors, non-epithelial cancer histology.

- Previous cancer diagnosis within the past five years or recurrent cancer

- Regular steroid use in the last month

- Presence of comorbidities with known effects on the immune system (e.g., systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis), congestive heart failure, pregnancy, or stroke within the past six months

- Major surgery in the past month.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Integrated psychological care
Additional possible strategies used may include supportive or validating interventions, increasing/introducing/reinforcing coping strategies, psychoeducation; distress tolerance skills; brief cognitive behavioral therapy; cognitive restructuring; activity scheduling; acceptance; and relaxation/mindfulness.
Other:
Surveys
NCCN Distress Thermometer PROMIS Depression & Anxiety Quality of Life (SF-12) Brief COPE Patient awareness and satisfaction survey
Procedure:
Blood draw
For patients with ovarian, fallopian tube, or primary peritoneal cysts Optional Enrollment, 3 months after enrollment, and 6 months after enrollment
Fresh tissue from ovary
For patients with ovarian, fallopian tube, or primary peritoneal cysts Optional At time of standard of care surgery

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine Barnes-Jewish Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility of integrating psychosocial care by a trained psychologist into gynecologic cancer outpatient clinics as measured by patient enrollment -Willingness to participate with integrated care as quantified by proportion of enrolled patients from the number of approached eligible patients Completion of patient enrollment (approximately 12 months)
Secondary Provider willingness to have a psychologist present -5 item survey about willingness to have psychologist present in clinic 6 months after start of study enrollment
Secondary Differences in clinic visit duration with and without a psychologist present -Clinic visit duration is defined as the time from check-in to patient discharge Day 1
Secondary Difference in psychological correlates of daily functioning as measured by patient distress between women who receive usual care versus integrated psychological care NCCN Distress Thermometer: picture of thermometer that states to circle the number that best describes how much distress has been experienced in the past week (10=extreme distress and 0=no distress)
Next section contains categories of Practical Problems, Family Problems, Emotional Problems, Physical Problems, Spiritual/religious concerns - participant is to mark yes or no to indicate if they have had problems in the past week
The distress thermometer score of 0-10 is recorded. The problem areas endorsements are tallied within each problem area.
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of daily functioning as measured by patient depression between women who receive usual care versus integrated psychological care PROMIS Depression & Anxiety - asks participant in the last 7 days if they have felt worthless, helpless, depressed, hopeless, fearful, lack of focus, worrying, and uneasy. Check box choices are never, rarely, sometimes, often, and always
Each question has five response options ranging in value from one to five. To find the total raw score for a short form with all questions answered, sum the values of the response to each question. Never = 1, rarely = 2, sometimes = 3, often =4, always = 5. Points are added to raw score. Raw score is converted to t-score via short form conversion table.
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of daily functioning as measured by patient anxiety between women who receive usual care versus integrated psychological care PROMIS Depression & Anxiety - asks participant in the last 7 days if they have felt worthless, helpless, depressed, hopeless, fearful, lack of focus, worrying, and uneasy. Check box choices are never, rarely, sometimes, often, and always
Point values are as follows: never =1, rarely, rarely = 2, sometimes = 3, often =4, always = 5. Points are added to raw score. Raw score is converted to t-score via short form conversion table.
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of daily functioning as measured by patient quality of life between women who receive usual care versus integrated psychological care Quality of life (SF-12): 12 item survey
Scores are recoded to give numerical value, with some items reverse scored. Scoring is broken down into mental health and physical health subscale scores.
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of daily functioning as measured by patient coping mechanisms between women who receive usual care versus integrated psychological care Brief COPE: 28 item survey with answers ranging from 1=I haven't been doing this at all to 4=I've been doing this a lot
Scores are on tallied based on answers to 4 point likert scale. No reverse scoring. There are 14 subscales with two questions each.
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of perception of psychological care as measured by patient perception of Siteman Cancer Center being highly focused on their wellbeing between women who receive usual care versus integrated psychological care 4 item survey
Each question has five response options ranging in value from one to five. To find the total raw score for a short form with all questions answered, sum the values of the response to each question.
1=strongly disagree to 5=strongly agree
Enrollment, 3 months after enrollment, and 6 months after enrollment
Secondary Difference in psychological correlates of awareness of psychological care as measured by awareness of support services offered between women who receive usual care versus integrated psychological care 4 item survey
Each question has five response options ranging in value from one to five. To find the total raw score for a short form with all questions answered, sum the values of the response to each question.
1=strongly disagree to 5=strongly agree
Enrollment, 3 months after enrollment, and 6 months after enrollment