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Spots Global Cancer Trial Database for Self-efficacy Coaching for Women With Breast Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Self-efficacy Coaching for Women With Breast Cancer

Official Title: Pilot Study: Individualized Self-efficacy Coaching, Quality of Life and Compliance for Women With High-risk Early Breast Cancer

Study ID: NCT03478384

Conditions

Breast Cancer

Interventions

Patient coaching

Study Description

Brief Summary: This is an open, prospective, multi-center, interventional study to evaluate the benefit and efficacy of individualized self-efficacy coaching for women with high-risk early breast cancer. In total, 6 sites will be assigned 1:1 to either the experimental arm (Group A) or the control arm (Group B). The controlled site assignment will assure a balanced site-specific QoL between both groups at baseline. All patients will be medically treated according to guidelines. The experimental Group A will in addition receive regular self-efficacy coaching.

Detailed Description: Breast cancer represents the leading cause of cancer in women in Switzerland with around 6,000 newly diagnosed cases per year. Beside the therapy- and cancer-associated somatic illness, about one third of patients develop anxiety disorders or depression and need psychotherapeutic or psychiatric care. Women with breast cancer display the highest psychic comorbidity compared to patients with other cancer entities (40% point prevalence) . To assist with psychological coping with the disease several psycho-oncological interventions have been established in the past decades. Self-efficacy describes the extent or strength of one's belief in one's own ability to complete tasks and reach goals. Nagel \& Schreiber have developed an individualized self-efficacy coaching for cancer patients to mobilize and strengthen the belief in one's own ability to deal with and fight the disease. The SECOM-PSWE study evaluates the impact of regular self-efficacy coaching on the perceived self-efficacy and the quality of life (QoL) in patients with early breast cancer.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Tumorzentrum ZeTuP Rapperswil-Jona, Rapperswil-Jona, Saint Gallen, Switzerland

Prolindo, Onkologie & Hämatologie, Team am Lindenhofspital, Bern, , Switzerland

Spital Thurgau AG - Kantonsspital Frauenfeld, Frauenfeld, , Switzerland

Hirslanden Klinik St. Anna, Luzern, , Switzerland

Tumor-und Brustzentrum ZeTuP AG St. Gallen, St. Gallen, , Switzerland

Stadtspital Triemli, Zürich, , Switzerland

Contact Details

Name: Gerd Nagel, Professor MD

Affiliation: Stiftung Patientenkompetenz

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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