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The self management of women with breast cancer - Enabling quality of life and participation

Does a 4 week self management program compared to usual care, improve the quality of life of women with breast cancer?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000712000
Acronym
SAMA= "Staying abreast, Moving ahead"
Enrollment
150
Registered
2010-08-27
Start date
2007-06-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Clinical Trial on patient self management for women with breast cancer to enable Quality of life (QOL) and Participation. The hypothesis is that the 4 week self management intervention will show statistical differences in the mean-score of the primary outcomes in the experimental groups

Interventions

Intervention is a 4-week self management program, led by a health care professional with a group of 8-12 patients who meet face-to-face, for 1 1/2 hours a week over 4 weeks. The intervention provides didactic and interactive session using behavioral interventions that focus on managing the medical, emotional and role tasks. It involves training self-management skills -(problem solving, decision making, resource utilization, the formation of a patient-provider partnership, action planning) to en

Intervention is a 4-week self management program, led by a health care professional with a group of 8-12 patients who meet face-to-face, for 1 1/2 hours a week over 4 weeks. The intervention provides didactic and interactive session using behavioral interventions that focus on managing the medical, emotional and role tasks. It involves training self-management skills -(problem solving, decision making, resource utilization, the formation of a patient-provider partnership, action planning) to enable women to self manage the illness and to improve health behavious. The duration (wash-out period) between experimental and control is 4 weeks.

Sponsors

University Malaya
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Participants must be newly diagnosed up to one year period, with stage 1-3 Breast cancer and able to give consent.

Exclusion criteria

Stage 4 Breast cancer Breast cancer recurrance Cognitively unable to participate

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026