search
Back to results

Nuevo Amanecer II: Translating a Stress Management Program for Latinas

Primary Purpose

Breast Neoplasms, Psychology, Social

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Nuevo Amancer-II Stress Management Program
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Neoplasms focused on measuring Breast cancer, Latinas, Peer support counselor, Spanish speaking, Community based, Rural

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Self-identifies as Latina
  • Diagnosed with Stage 0, I, II, or III (non-metastatic) breast cancer
  • Primarily Spanish-speaking, or Spanish monolingual
  • Aged 18 or older
  • Living in surrounding areas of Tulare (Visalia, Dinuba), Santa Cruz (Eastside Santa Cruz, Watsonville, Freedom), or Imperial Valley (El Centro) counties, California.

Exclusion Criteria:

  • Terminal illness
  • Stage IV breast cancer (distant metastasis)

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Nuevo Amancer-II Stress Management Program

Wait-list Control Group

Arm Description

Nuevo Amanecer-II (NA-II) is a 10-week peer-delivered cognitive-behavioral stress management program. Participants receive the stress management program as soon as possible after randomization.

Waits six months and at the end of the six months is offered the option of receiving the NA-II program.

Outcomes

Primary Outcome Measures

Change in Physical Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Change in Social/Family Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Change Emotional Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Change in Breast Cancer Concerns Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Change in Functional Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Change in Total Score of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)

Secondary Outcome Measures

Change Anxiety Score, a Subscale of the Brief Symptom Inventory (BSI)
Change Somatization Score, a Subscale of the Brief Symptom Inventory (BSI)
Change in Personal Health Questionnaire Depression Scale (PHQ-8) Score
Change Perceived Stress Scale (PSS-10) Score
Change MOS Health Distress Scale Score
Change in long-term stress level measured by cortisol levels collected from hair sample.
Study staff will collect hair sample pre-intervention (baseline) and at the 6-month follow-up. All hair samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff for cortisol characterization.
Change in telomere length, a measure of biological aging, in DNA collected from saliva sample.
Study staff will collect a saliva sample pre-intervention (baseline) and at the 6-month follow-up. All saliva samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff to process to extract DNA and measure telomeres.
Change in diurnal cortisol rhythm to assess regulatory patterns through saliva samples collected over 3 days, 3 times/day.
Participants will collect nine saliva samples pre-invention (baseline) and at the 6-month follow-up. The first two samples will be taken within the first half hour of waking (first upon awakening and 30 minutes after waking). Participants will collect the last sample right before they go to bed. All saliva samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff for cortisol characterization.

Full Information

First Posted
October 11, 2016
Last Updated
April 3, 2019
Sponsor
University of California, San Francisco
Collaborators
California Breast Cancer Research Program, National Institute on Aging (NIA), Circulo de Vida Cancer Support and Resource Center, Cancer Resource Center of the Desert, Family Service Agency of the Central Coast, Kaweah Delta Health Care District, San Francisco State University
search

1. Study Identification

Unique Protocol Identification Number
NCT02931552
Brief Title
Nuevo Amanecer II: Translating a Stress Management Program for Latinas
Official Title
Translating a Stress Management Program for Latinas
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
October 2018 (Actual)
Study Completion Date
February 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
California Breast Cancer Research Program, National Institute on Aging (NIA), Circulo de Vida Cancer Support and Resource Center, Cancer Resource Center of the Desert, Family Service Agency of the Central Coast, Kaweah Delta Health Care District, San Francisco State University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary aim is to assess the effectiveness of the Nuevo Amanecer-II (NA-II) cognitive-behavioral stress management program through a 6-month RCT with 150 Spanish-speaking Latinas with breast cancer in three rural settings in terms of improving quality of life (QoL) and reducing distress, compared to a usual care control group (that is offered the program at the end of the 6 months). The investigators will also test the effects of the program on biomarkers of stress (hair and saliva cortisol) and aging (telomere length from saliva). Trained Latinas, called Compañeras (Companions), who have had breast cancer deliver the stress management program in-person to Spanish-speaking Latinas with breast cancer.
Detailed Description
The purpose of this study is to adapt Nuevo Amanecer (NA-I) for use in rural populations and test the effects of the new adapted program, NA-II, in a 6-month RCT among 150 rural, low literacy Latinas with non-metastatic breast cancer. Primary outcomes will consist of quality of life and distress. In an ancillary study, the investigators will compare the intervention and wait-list control groups on biomarkers of stress (hair and saliva cortisol) and aging (telomere length from saliva). Finally, to facilitate statewide dissemination of Nuevo Amanecer-II (NA-II), the investigators will develop a guide to implementation for community-based organizations. The investigators will adapt NA-I to be appropriate for rural and low-literacy Latinas with breast cancer. Needed program adaptations will be identified through a formative evaluation consisting of semi-structured interviews with key informants (e.g., rural Latina breast cancer survivors, advocates, health care providers) and iterative consultations with community representatives in three rural areas with large Latino populations. Results will be applied by the study team and community advisors to adapt NA-I to create NA-II and create the implementation guide. The investigators will identify key individual, organizational, and community factors that facilitate implementation and support scalability and statewide dissemination through a process evaluation where the investigators will track key implementation activities and debrief program participants, interventionists, and advocates. Products will include NA-II interventionist and participant manuals and a guide to implementation for organizations seeking to replicate the program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasms, Psychology, Social
Keywords
Breast cancer, Latinas, Peer support counselor, Spanish speaking, Community based, Rural

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
153 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nuevo Amancer-II Stress Management Program
Arm Type
Experimental
Arm Description
Nuevo Amanecer-II (NA-II) is a 10-week peer-delivered cognitive-behavioral stress management program. Participants receive the stress management program as soon as possible after randomization.
Arm Title
Wait-list Control Group
Arm Type
No Intervention
Arm Description
Waits six months and at the end of the six months is offered the option of receiving the NA-II program.
Intervention Type
Behavioral
Intervention Name(s)
Nuevo Amancer-II Stress Management Program
Other Intervention Name(s)
Nuevo Amanecer II (A New Dawn) cognitive-behavioral stress management program
Intervention Description
Participant meets weekly with a trained interventionist called a Compañera (a peer who has had breast cancer) to complete a structured 10-week program designed to develop cognitive and behavioral skills to manage stress and distress, improve communication with family and clinicians, and increase knowledge of self-management after breast cancer.
Primary Outcome Measure Information:
Title
Change in Physical Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Title
Change in Social/Family Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Title
Change Emotional Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Title
Change in Breast Cancer Concerns Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Title
Change in Functional Well-being Score, a Subscale of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Title
Change in Total Score of the Functional Assessment of Cancer Therapy-Breast Quality of Life Instrument (FACT-B)
Time Frame
Baseline and 6 month assessment
Secondary Outcome Measure Information:
Title
Change Anxiety Score, a Subscale of the Brief Symptom Inventory (BSI)
Time Frame
Baseline and 6 month assessment
Title
Change Somatization Score, a Subscale of the Brief Symptom Inventory (BSI)
Time Frame
Baseline and 6 month assessment
Title
Change in Personal Health Questionnaire Depression Scale (PHQ-8) Score
Time Frame
Baseline and 6 month assessment
Title
Change Perceived Stress Scale (PSS-10) Score
Time Frame
Baseline and 6 month assessment
Title
Change MOS Health Distress Scale Score
Time Frame
Baseline and 6 month assessment
Title
Change in long-term stress level measured by cortisol levels collected from hair sample.
Description
Study staff will collect hair sample pre-intervention (baseline) and at the 6-month follow-up. All hair samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff for cortisol characterization.
Time Frame
Baseline and 6 month assessment
Title
Change in telomere length, a measure of biological aging, in DNA collected from saliva sample.
Description
Study staff will collect a saliva sample pre-intervention (baseline) and at the 6-month follow-up. All saliva samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff to process to extract DNA and measure telomeres.
Time Frame
Baseline and 6 month assessment
Title
Change in diurnal cortisol rhythm to assess regulatory patterns through saliva samples collected over 3 days, 3 times/day.
Description
Participants will collect nine saliva samples pre-invention (baseline) and at the 6-month follow-up. The first two samples will be taken within the first half hour of waking (first upon awakening and 30 minutes after waking). Participants will collect the last sample right before they go to bed. All saliva samples will then be picked up by San Francisco State University Health Equity Research Laboratory (HER) staff for cortisol characterization.
Time Frame
Baseline and 6 month assessment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Self-identifies as Latina Diagnosed with Stage 0, I, II, or III (non-metastatic) breast cancer Primarily Spanish-speaking, or Spanish monolingual Aged 18 or older Living in surrounding areas of Tulare (Visalia, Dinuba), Santa Cruz (Eastside Santa Cruz, Watsonville, Freedom), or Imperial Valley (El Centro) counties, California. Exclusion Criteria: Terminal illness Stage IV breast cancer (distant metastasis)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Gregorich, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
City
Multiple Locations
State/Province
California
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35967922
Citation
Samayoa C, Santana-Ufret V, Santoyo-Olsson J, Strassle PD, Stewart A, Bonilla J, Escalera C, Mendez RM, Marquez-Magana L, Ortiz C, Ceballos RM, Napoles AM. Cortisol levels in rural Latina breast cancer survivors participating in a peer-delivered cognitive-behavioral stress management intervention: The Nuevo Amanecer-II RCT. Compr Psychoneuroendocrinol. 2022 Jun 24;11:100153. doi: 10.1016/j.cpnec.2022.100153. eCollection 2022 Aug.
Results Reference
derived
PubMed Identifier
34998436
Citation
Bonilla J, Alhomsi A, Santoyo-Olsson J, Stewart AL, Ortiz C, Samayoa C, Torres-Nguyen A, Palomino H, Coleman V, Urias A, Gonzalez N, Cervantes SA, Duron Y, Napoles AM. Sharing research results with Latina breast cancer survivors who participated in a community-engaged behavioral RCT study: a descriptive cross-sectional survey study. Trials. 2022 Jan 8;23(1):25. doi: 10.1186/s13063-021-05945-8.
Results Reference
derived
PubMed Identifier
33563263
Citation
Bonilla J, Escalera C, Santoyo-Olsson J, Samayoa C, Ortiz C, Stewart AL, Napoles AM. The importance of patient engagement to quality of breast cancer care and health-related quality of life: a cross-sectional study among Latina breast cancer survivors in rural and urban communities. BMC Womens Health. 2021 Feb 9;21(1):59. doi: 10.1186/s12905-021-01200-z.
Results Reference
derived
PubMed Identifier
32132128
Citation
Samayoa C, Santoyo-Olsson J, Escalera C, Stewart AL, Ortiz C, Marquez-Magana L, Urias A, Gonzalez N, Cervantes SA, Torres-Nguyen A, Parada-Ampudia L, Napoles AM. Participant-Centered Strategies for Overcoming Barriers to Biospecimen Collection among Spanish-Speaking Latina Breast Cancer Survivors. Cancer Epidemiol Biomarkers Prev. 2020 Mar;29(3):606-615. doi: 10.1158/1055-9965.EPI-19-0942.
Results Reference
derived

Learn more about this trial

Nuevo Amanecer II: Translating a Stress Management Program for Latinas

We'll reach out to this number within 24 hrs