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Yoga for Psychological Distress in Gynecologic, Gastrointestinal, or Thoracic Cancer

Primary Purpose

Gynecologic Cancer, Adjustment, Gastrointestinal Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Stilling the Waters of Uncertainty: A yoga program for women with gynecologic, gastrointestinal (GI), or thoracic cancer
Sponsored by
University of Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Gynecologic Cancer focused on measuring Gastrointestinal (GI), Fear of Cancer Recurrence (FCR)

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Presence of newly diagnosed
  • pathology-confirmed
  • (a) gynecologic cancer (e.g., cancer of the ovaries, cervix, endometrium, fallopian tubes), any stage, or
  • (b) borderline ovarian tumor, Stage II-III
  • Undergoing (or have recently undergone) surgery and/or active cancer treatment (e.g., chemotherapy, radiation, a combination of these treatments and/or another form of cancer treatment)
  • Able to read and write in English

Exclusion Criteria:

  • History of gynecologic cancer or other cancer diagnosis (excluding basal cell or squamous cell carcinomas of the skin)
  • Current, severe, uncontrolled psychopathology (e.g., symptomatic Bipolar Disorder with a manic or depressive episode in the last six months, psychotic symptoms or disorder, or documented personality disorder)
  • History of dementia or other neurocognitive disorder that may interfere with participants' ability to adhere to study procedures
  • Poor performance status as determined by a Karnofsky Status Score < 60,
  • For those with any childbearing potential (i.e., 18 - 62 years of age, have intact reproductive organs, and/or have not yet started chemotherapy or radiation therapy): self-reported current pregnancy, possible pregnancy, or efforts to become pregnant
  • History of regular or immersive yoga practice in the last five years defined as attending at least once weekly yoga classes for at least 6 consecutive months at any point in the prior 5 years

Sites / Locations

  • University of Florida

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Yoga Intervention

Arm Description

The intervention, "Stilling the Waters of Uncertainty: A yoga program for women with gynecologic, gastrointestinal (GI), or thoracic cancer," is a 10-week, manualized, group yoga program. Sessions are 60 minutes in duration, once a week, across the course of 10 weeks. The 10-week program is comprised of five modules, each of which will take two sessions to complete: (1) Getting Started, (2) Cultivating a Mindful Attitude, (3) Self-Care and Compassion, (4) Finding Peace and Acceptance, and (5) The Power of the Present Moment.

Outcomes

Primary Outcome Measures

Feasibility of the proposed yoga program - Study enrollment rate
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Feasibility of the proposed yoga program - Intervention session attendance
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Feasibility of the proposed yoga program - Adherence to homework assignments
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Feasibility of the proposed yoga program - Retention through follow-up assessment (i.e., individuals who complete all components of the study)
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Feasibility of the proposed yoga program - Safety (i.e., adverse events)
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility
Program Acceptability- Relevance of the intervention to their lives
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Program Acceptability- the Utility of the intervention to participants
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Program Acceptability- Satisfaction/Enjoyment of the intervention
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Program Acceptability - Clarity/Ease of the intervention for participants
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Program Acceptability - Plan to continue intervention exercises after completion of the study
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.

Secondary Outcome Measures

Fear of Cancer Recurrence (FCR)
This measure will access participants' Fear of Cancer Recurrence (FCR), which includes cognitive, behavioral, and emotional experiences related to worries that their cancer will return.
Cancer-Related Distress
The Distress Thermometer will be used to assess cancer-related distress. This measure is designed to assess self-efficacy regarding distress and symptom management while facing a cancer diagnosis. Domains assessed include maintenance of activity and independence, seeking and understanding medical information, stress management, coping with treatment side effects, maintaining a positive attitude, engaging in emotion regulation, and seeking support.
State and Trait Anxiety
Anxiety will be assessed with the State Trait Anxiety Inventory (STAI) Assesses state /trait anxiety symptoms on 4 pt. likert scale. Medium: May indicate anxiety disorder
Depressive Symptoms
Depressive symptoms will be assessed with the Beck Depression Inventory - Second Edition (BDI-2) - high score Suicidal Behavior

Full Information

First Posted
December 20, 2017
Last Updated
June 13, 2023
Sponsor
University of Florida
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1. Study Identification

Unique Protocol Identification Number
NCT03385577
Brief Title
Yoga for Psychological Distress in Gynecologic, Gastrointestinal, or Thoracic Cancer
Official Title
Feasibility, Acceptability, and Efficacy of a Yoga Intervention for Distress in Women With Gynecologic, Gastrointestinal, or Thoracic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
February 5, 2018 (Actual)
Primary Completion Date
November 14, 2022 (Actual)
Study Completion Date
November 14, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will test the feasibility and acceptability of a yoga program for women with gynecologic, gastrointestinal (GI), or thoracic malignancies. This study will pilot an integrative yoga intervention that combines Western psychotherapeutic approaches with classic yogic philosophy to reduce emotional distress among women undergoing treatment for gynecologic, gastrointestinal (GI), or thoracic cancer and provide a comprehensive approach to stress management across the cancer care continuum.
Detailed Description
Gynecologic cancers are malignancies of the female reproductive tract that affect over 70,000 women per year. Treatments for gynecologic cancer often result in numerous physical and emotional side effects that affect long-term adjustment, such as anxiety, depression, low self-esteem, sexual dysfunction, difficulties with fertility, and surgically-induced menopause. Even when initial treatments are successful, gynecologic cancers have a high recurrence rate that can reach nearly 80% among those with ovarian cancer. Fear of Cancer Recurrence (FCR) is described as one of the largest unmet psychological needs among gynecologic cancer patients and is associated with psychological distress, increased health care utilization, and functional impairment. Few studies have examined interventions designed to manage symptoms of FCR, which leaves a significant gap in the literature regarding treatment of this prominent psychosocial problem. Cancer patients report growing use of integrative medicine therapies (e.g., yoga, acupuncture, massage) to manage unmet physical and emotional needs related to their disease and treatment. The current study will take advantage of this trend in supportive oncology to investigate the feasibility and acceptability of a novel intervention program created specially to address FCR among women with gynecologic cancer. Patients will be recruited from the UF Health/Shands Hospital Gynecology Oncology Clinic and Medical Oncology clinic and invited to participate in a 10-week, manualized, small group yoga course. Psychoeducation modules, meditation training, and gentle yoga poses will be integrated into a comprehensive program focused on managing the psychosocial concerns of newly diagnosed gynecologic cancer patients. Findings from this research will contribute to the existing literature on FCR and knowledge regarding the use of integrative medicine techniques for addressing unmet psychological needs among gynecologic cancer patients. If the intervention is deemed feasible and acceptable, future research may explore ways in which this manualized yoga program compares to other psychosocial treatments for managing FCR and other forms of emotional distress in women with cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gynecologic Cancer, Adjustment, Gastrointestinal Cancer, Thoracic Cancer
Keywords
Gastrointestinal (GI), Fear of Cancer Recurrence (FCR)

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
125 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Yoga Intervention
Arm Type
Experimental
Arm Description
The intervention, "Stilling the Waters of Uncertainty: A yoga program for women with gynecologic, gastrointestinal (GI), or thoracic cancer," is a 10-week, manualized, group yoga program. Sessions are 60 minutes in duration, once a week, across the course of 10 weeks. The 10-week program is comprised of five modules, each of which will take two sessions to complete: (1) Getting Started, (2) Cultivating a Mindful Attitude, (3) Self-Care and Compassion, (4) Finding Peace and Acceptance, and (5) The Power of the Present Moment.
Intervention Type
Behavioral
Intervention Name(s)
Stilling the Waters of Uncertainty: A yoga program for women with gynecologic, gastrointestinal (GI), or thoracic cancer
Intervention Description
'Stilling the waters,' the prominent theme of this program, is drawn from the core principle in yogic philosophy. It uses breath techniques and physical postures to cultivate inner peace and an ability to live in the present moment. The emphasis on stilling the fluctuations of uncertainty is a direct allusion to the intrusive and inherently unknown future, which characterizes the core experience of Fear of Cancer Recurrence (FCR). This is especially true among gynecologic, gastrointestinal (GI), or thoracic cancer patients for whom the likelihood of recurrence is quite high. An additional motif throughout the program is the lotus flower. The symbolic importance of the lotus in yogic culture is due to its requiring thick muddy waters for ideal growth. The metaphor of cancer as the muddy waters will be used to cultivate benefit-finding and acceptance regarding the mental and physical challenges participants endured during their initial diagnosis and treatment.
Primary Outcome Measure Information:
Title
Feasibility of the proposed yoga program - Study enrollment rate
Description
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Feasibility of the proposed yoga program - Intervention session attendance
Description
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Feasibility of the proposed yoga program - Adherence to homework assignments
Description
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Feasibility of the proposed yoga program - Retention through follow-up assessment (i.e., individuals who complete all components of the study)
Description
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Feasibility of the proposed yoga program - Safety (i.e., adverse events)
Description
Patients will complete the majority (80%) of study activities as measured by five empirically-driven indicators of feasibility
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Program Acceptability- Relevance of the intervention to their lives
Description
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Program Acceptability- the Utility of the intervention to participants
Description
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Program Acceptability- Satisfaction/Enjoyment of the intervention
Description
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Program Acceptability - Clarity/Ease of the intervention for participants
Description
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Program Acceptability - Plan to continue intervention exercises after completion of the study
Description
The majority of patients (80%) will rate five key dimensions of the intervention on a Likert scale as "Very" or "Extremely" acceptable.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Secondary Outcome Measure Information:
Title
Fear of Cancer Recurrence (FCR)
Description
This measure will access participants' Fear of Cancer Recurrence (FCR), which includes cognitive, behavioral, and emotional experiences related to worries that their cancer will return.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Cancer-Related Distress
Description
The Distress Thermometer will be used to assess cancer-related distress. This measure is designed to assess self-efficacy regarding distress and symptom management while facing a cancer diagnosis. Domains assessed include maintenance of activity and independence, seeking and understanding medical information, stress management, coping with treatment side effects, maintaining a positive attitude, engaging in emotion regulation, and seeking support.
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
State and Trait Anxiety
Description
Anxiety will be assessed with the State Trait Anxiety Inventory (STAI) Assesses state /trait anxiety symptoms on 4 pt. likert scale. Medium: May indicate anxiety disorder
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)
Title
Depressive Symptoms
Description
Depressive symptoms will be assessed with the Beck Depression Inventory - Second Edition (BDI-2) - high score Suicidal Behavior
Time Frame
Pre-Intervention (Baseline) to Post-Intervention (Ten Weeks After Baseline)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of newly diagnosed pathology-confirmed (a) gynecologic cancer (e.g., cancer of the ovaries, cervix, endometrium, fallopian tubes), any stage, or (b) borderline ovarian tumor, Stage II-III Undergoing (or have recently undergone) surgery and/or active cancer treatment (e.g., chemotherapy, radiation, a combination of these treatments and/or another form of cancer treatment) Able to read and write in English Exclusion Criteria: History of gynecologic cancer or other cancer diagnosis (excluding basal cell or squamous cell carcinomas of the skin) Current, severe, uncontrolled psychopathology (e.g., symptomatic Bipolar Disorder with a manic or depressive episode in the last six months, psychotic symptoms or disorder, or documented personality disorder) History of dementia or other neurocognitive disorder that may interfere with participants' ability to adhere to study procedures Poor performance status as determined by a Karnofsky Status Score < 60, For those with any childbearing potential (i.e., 18 - 62 years of age, have intact reproductive organs, and/or have not yet started chemotherapy or radiation therapy): self-reported current pregnancy, possible pregnancy, or efforts to become pregnant History of regular or immersive yoga practice in the last five years defined as attending at least once weekly yoga classes for at least 6 consecutive months at any point in the prior 5 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deidre B. Pereira, PhD
Organizational Affiliation
University of Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35651964
Citation
Hanvey GA, Padron A, Kacel EL, Cartagena G, Bacharz KC, McCrae CS, Robinson ME, Waxenberg LB, Antoni MH, Berry RB, Schultz GS, Castagno J, Pereira DB. Accrual and retention of diverse patients in psychosocial cancer clinical trials. J Clin Transl Sci. 2022 Apr 1;6(1):e45. doi: 10.1017/cts.2022.380. eCollection 2022.
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Yoga for Psychological Distress in Gynecologic, Gastrointestinal, or Thoracic Cancer

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