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A Novel Prosocial Online Support Group for Distressed Breast Cancer Survivors

A Novel Prosocial Online Support Group for Distressed Breast Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01396174
Enrollment
184
Registered
2011-07-18
Start date
2011-08-31
Completion date
2014-11-30
Last updated
2015-04-17

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

Conditions

Breast Neoplasms

Keywords

breast cancer, breast tumor

Brief summary

The investigators hypothesize that breast cancer survivors participating in a prosocial online support group will have a significantly lower mean level of psychological symptoms (anxiety/depression) and higher mean level of sense of purpose post-intervention than participants in a standard online support group.

Detailed description

Psychological distress is a significant problem among breast cancer survivors. Many survivors turn to the internet for information and support, yet few controlled studies have examined the effectiveness and safety of online support groups. The investigators are testing the potential efficacy, acceptability, and feasibility of an innovative theory-based online support group (OSG) for breast cancer survivors. Members of the control group will participate in a standard OSG that encourages self-expression. Members of the experimental condition will participate in a prosocial OSG that provides structured helping opportunities and coaching on how best to give support to others. Participants will complete two telephone interviews and six weekly online support group meetings.

Interventions

BEHAVIORALprosocial online support group

Six weekly 1.5 hour online support group meetings facilitated by a Cancer Support Community staff member. This online support group will maximize opportunities to provide help to others.

BEHAVIORALStandard Online Support Group

Six weekly 1.5 hour online support group meetings facilitated by a Cancer Support Community staff member. This online support group will focus on encouraging self-expression.

Sponsors

Cancer Support Community, Research and Training Institute, Philadelphia
CollaboratorOTHER
Temple University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* diagnosed with stage I or II breast cancer in preceding 36 months * 21-64 years of age * access to and ability to use a computer and the internet to communicate with others * fluent in spoken English * meet the screening criteria for psychological distress (score \>7 on either the depression or anxiety subscale of the Hospital Anxiety and Depression Scales

Exclusion criteria

* currently taking medication for depression

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety and Depression Scalechange from baseline to one month post-intervention

Secondary

MeasureTime frameDescription
Sense of Coherence measurechange from baseline to one month post-interventionWe are using the Meaningfulness/Purpose in Life subscale of the Sense of Coherence measure to assess sense of purpose.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026