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ExBRAC- Expressive Writing in Breast Cancer

Expressive Writing in Breast Cancer - The ExBRAC Trial

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07298980
Acronym
ExBRAC
Enrollment
272
Registered
2025-12-23
Start date
2026-02-01
Completion date
2029-12-31
Last updated
2026-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

breast cancer, quality of life, expressive writing

Brief summary

The study is a randomized trial designed to examine whether an "expressive writing" intervention can affect the quality of life in patients recently diagnosed with breast cancer. The method "expressive writing" consists of writing about the breast cancer or other related subjects during 20 minutes, once a week for four consecutive weeks. The impact on quality of life will be assessed by having participants complete questionnaires at three different time points during the study. The questionnaire will be developed using a clinimetric approach, based on semi-structured interviews with breast cancer patients. The themes emerging from these interviews will be used to formulate the questions. Additionally, well-known quality-of-life measurement instruments and registry data with clinically relevant information-such as tumor stage and treatment-will be incorporated.

Interventions

BEHAVIORALExpressive Writing

Expressive writing means that the patient writes privately about the cancer or other related subject for 20 minutes. This will be repeated once a week for 4 weeks. The writing should be done in a place free from distractions and on the patients' mother tongue. The text will not be collected.

Sponsors

Region Skane
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned for surgery of breast cancer without neoadjuvant treatment

Exclusion criteria

* Not able to understand Swedish * Previous breast cancer

Design outcomes

Primary

MeasureTime frameDescription
Health-related quality of lifeAt the 12 months follow-upAccording to EQ-5D-5L VAS. The scale ranges from 0-100 where 0 is "worst possible health" and 100 is "best possible health".

Countries

Sweden

Contacts

PRINCIPAL_INVESTIGATORLinnea Huss, M.D., Ph.D.

Lund University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026