Stopped: The recruitment for the study slowed and funding for the study has completed.
The purpose of this two-arm pilot RCT is to evaluate processes and preliminary outcomes of a targeted QOL intervention vs. an attention control among young AA survivors post-treatment for early (I-II) \& late (III) stage breast cancer.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Proportion of screen-eligible patients enrolled by consent
Timeframe: Up to 2 years
Proportion of patients that complete all (five) study contacts of intervention
Timeframe: Up to 2 years
Acceptability/Relevance of Intervention Sessions
Timeframe: Up to 2 years
Participation in aspects of protocol
Timeframe: Up to 2 years
Use of proposed self-management strategies and perceived effectiveness
Timeframe: Up to 2 years
Medical Outcomes Survey Short-Form (SF-36)
Timeframe: Baseline up to 1 month post-intervention
PROMIS Global Health10
Timeframe: Baseline up to 1 month post-intervention
(Functional Assessment of Chronic Illness Therapy Spiritual Well-Being (FACT-Sp 12)
Timeframe: Baseline up to 1 month post-intervention
MOS Modified Social Support Survey
Timeframe: Baseline up to 1 month post-intervention
PROMIS Applied Cognition - General Concerns short form (8- item)
Timeframe: Baseline up to 1 month post-intervention