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A Novel Prosocial Online Support Group for Distressed Breast Cancer Survivors

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Temple University

Status

Completed

Conditions

Breast Neoplasms

Treatments

Behavioral: Standard Online Support Group
Behavioral: prosocial online support group

Study type

Interventional

Funder types

Other

Identifiers

NCT01396174
RCA158877A

Details and patient eligibility

About

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.

Full 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.

Enrollment

184 patients

Sex

Female

Ages

21 to 64 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

184 participants in 2 patient groups

Standard Online Support Group
Active Comparator group
Treatment:
Behavioral: Standard Online Support Group
Prosocial Online Support Group
Experimental group
Treatment:
Behavioral: prosocial online support group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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