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Effectiveness of Peer Support on Quality of Life in Recently Diagnosed Breast Cancer Patients

Effectiveness of Peer Support on Quality of Life in Recently Diagnosed Breast Cancer Patients - a Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03394742
Enrollment
260
Registered
2018-01-09
Start date
2014-05-01
Completion date
2016-10-30
Last updated
2018-01-09

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

Conditions

Breast Cancer

Keywords

Peer Group, Quality of Life

Brief summary

This study examines effectiveness of peer support of breast cancer patients. Half of the participants received peer support via telephone in addition to usual care and another half are give the usual care only.

Detailed description

Seriously sick people need social support to maintain their quality of life. Social support may be given by peers, who have experienced the same. In this study voluntary participants with recently diagnosed breast cancer were randomly allocated to intervention (N=130) or control (N=130) group. The intervention group received, in addition to usual care, peer support via telephone 1-5 times according to their own preference. The control group received usual care only. Peer support was given by volunteered breast cancer survivors who were educated for giving peer support.

Interventions

BEHAVIORALPeer support

Peer support persons are breast cancer survivors, who were educated to give peer support. They contacted participants by telephone.

Sponsors

Helsinki University Central Hospital
CollaboratorOTHER
University of Jyvaskyla
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* recently diagnosed primary breast cancer * no other serious illnesses * ability to communicate in Finnish or Swedish (official languages in Finland) * ability to fill in the questionnaires

Exclusion criteria

* some other serious illnesses * inability to communicate in Finnish or Swedish (official languages in Finland) * inability to fill in the questionnaires

Design outcomes

Primary

MeasureTime frameDescription
A change of health-related quality of life (HRQoL).From baseline to 3, 6 and 12 months later.HRQoL was assessed with a generic 15D instrument.

Secondary

MeasureTime frameDescription
Satisfaction for lifeBaseline and 3, 6 and 12 months later.Satisfaction for life was assessed with a questionnaire created for this study.
The use of health care servicesBaseline and 3, 6 and 12 months later.The use of health care services was assessed with a questionnaire create for this study.

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026