Project SOAR Awakenings for Black American women with breast cancer

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Project SOAR Awakenings is a randomized, controlled intervention comparing an online psychoeducational/psychosocial program to a mailed-materials comparison condition for Black American women with breast cancer. Eligible participants complete an electronic baseline questionnaire and standardized measures of depressive symptoms, fatigue, and well-being, as well as potential mediators like self-compassion and coping styles. Recruitment is conducted through Carrie's TOUCH and affiliated AME church networks, and the intervention is delivered online (Zoom) while the comparison group receives mailed materials to use on their own. Outcomes for the two groups will be compared to see if the online Awakenings program leads to greater improvements in mood, fatigue, and overall well-being.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* identifying as a woman at least 18 years of age (not limited to cisgender Black American women);
* identifying as Black (African) American;
* diagnosed with breast cancer of any stage and any diagnosis duration;
* able to speak and read English;
* residing in the United States;
* access to the internet/Zoom.

Exclusion Criteria:

* men diagnosed with breast cancer,
* non-English speaker
* nonresident of the United States
* no internet access

Where it's running

• UCLA
  Los Angeles, California, United States Recruiting

Study contacts

• Principal investigator: Annette L Stanton, PhD — University of California, Los Angeles
• Study coordinator: Alexandra Jorge, MA
• Email: projectsoar2018@gmail.com
• Phone: 323-425-9379

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Gyrotonic exercise for elders with breast cancer and Behcet disease

  We’re testing whether a gyrotonic exercise program helps older people who have both Behcet disease and breast cancer.

  Recruiting Cairo University · Giza, Dokki · NCT07929116

• PECS II vs SPSIP nerve blocks for pain after mastectomy

  This study tests whether two ultrasound-guided nerve blocks (PECS II and SPSIP) differ in how much opioid patients need after mastectomy.

  Recruiting Bursa City Hospital · Nilufer, Bursa · NCT07929090

• CG-7321: a first-in-human test in advanced solid tumors

  We’re testing CG-7321 alone and with fulvestrant to see if it’s safe and tolerable in adults with advanced solid tumors.

  Recruiting at 4 sites Phase 1 Chengdu Cynogen Bio-pharmaceutical Tech. Co., Ltd. · Fuzhou, Fujian and 3 other locations · NCT07923214

• Compare a new endoscopy-assisted breast-conserving surgery with the usual approach

  This study tests whether a new endoscopy-assisted breast-conserving technique can provide similar or better cosmetic outcomes and safety compared with conventional breast-conserving surgery in women with early breast cancer who want to preserve their breast.

  Recruiting Sir Run Run Shaw Hospital · Hangzhou, Zhejiang and 21 other locations · NCT07920094

• Different skin care approaches to prevent skin reactions after mastectomy radiation

  This study tests three standard skin care methods to see which best prevents radiation dermatitis in people who had a mastectomy and are receiving post-mastectomy radiation therapy.

  Recruiting at 7 sites Phase 2 Memorial Sloan Kettering Cancer Center · Basking Ridge, New Jersey and 6 other locations · NCT07918989

• 3D Heart Strain to Detect Early Cardiotoxicity in Cancer Therapy

  This study tests whether 3D echocardiography can detect early heart damage from cancer treatments like anthracyclines or HER2-targeted therapy better than standard 2D methods.

  Recruiting Region Skane · Lund, Skåne County · NCT07916337

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.