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Pain Coping Skills Training (PCST) / Breast Cancer · Interventional Study
ClinicalTrials.gov · August 12, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a planned randomized controlled trial of a brief telehealth pain coping skills training intervention for women with breast cancer in underserved settings, with estimated enrollment of 168 participants. No results have been posted to the registry; the study is currently recruiting. Primary outcomes include pain severity and interference (Brief Pain Inventory) and health-related quality of life (PROMIS-29 physical and mental health subscales) measured at baseline, 10 weeks, and 15 weeks.
Interventional, Randomized, Parallel, Open label, Supportive Care purpose. Breast Cancer; Female; age from 55 Years. Intervention: Pain Coping Skills Training. Compared with: Usual Care — No Intervention. n = 168. 1 site: United States.
This is a planned randomized controlled trial of a brief telehealth pain coping skills training intervention for women with breast cancer in underserved settings, with estimated enrollment of 168 participants. No results have been posted to the registry; the study is currently recruiting. Primary outcomes include pain severity and interference (Brief Pain Inventory) and health-related quality of life (PROMIS-29 physical and mental health subscales) measured at baseline, 10 weeks, and 15 weeks.
This is a registry record with no results posted; no efficacy, safety, or outcome data are available. Blinding status, adverse event monitoring, and secondary outcomes not detailed in the registry record.
The source did not state who this applies to in practice.
This is a registered but not yet completed trial with no results posted; it describes a planned intervention study in an underserved population with patient-reported outcomes as primary endpoints.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07300995). This is a study registration, not published results. Lead sponsor: Weill Medical College of Cornell University. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 168 participants (ESTIMATED). Conditions: Breast Cancer. Interventions: BEHAVIORAL: Pain Coping Skills Training (PCST). Primary outcome measures: Pain severity as measured by the Brief Pain Inventory (BPI) , Baseline, 10-week assessment, 15-week assessment; Pain interference as measured by the Brief Pain Inventory (BPI) , Baseline, 10-week assessment, 15-week assessment; Health Related Quality of Life (HR-QOL) as measured by the Patient Reported Outcomes Measurement Information System (PROMIS-29) - Physical Function , Baseline, 10-week assessment, 15-week assessment; Health Related Quality of Life (HR-QOL) as measured by the Patient Reported Outcomes Measurement Information System (PROMIS-29) - Mental Health , Baseline, 10-week assessment, 15-week assessment. Brief summary: This randomized controlled trial examines a 1-session, telehealth pain coping skills training (PCST) protocol with five 15-minute maintenance calls (Brief PCST-Community) adapted for women with breast cancer in medically underserved areas. Pain, health-related quality of life, and self-efficacy for pain management will be assessed at baseline and 10 and 15 weeks later.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.