Impact of a Rehabilitation Programme for Mothers With Breast Cancer and Their Children

NCT00916825 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 801

Last updated 2019-04-17

No results posted yet for this study

Summary

About 1/3 of newly diagnosed breast cancer patients are mothers of children who still live at home. They face additional challenges and stress, their children are also affected by the mother's illness. The oncological rehabilitation programme "getting better together" focuses on these special family needs. This waiting-control-group study examines the effectiveness of the intervention by accompanying the patients and their children over the course of a year and assessing their quality of life and psychological health.

Conditions

Interventions

BEHAVIORAL

rehabilitation programme "getting better together"

Mothers and their children (age 0-16) take part in a 3-week, family-oriented oncological rehabilitation programme which consists of medical, psychological and psychooncological treatments for mothers and children.

Sponsors & Collaborators

  • Dept. of Child and Adolescent Psychiatry, Philipps University Marburg

    collaborator OTHER
  • Rexrodt von Fircks Foundation

    collaborator UNKNOWN
  • Philipps University Marburg

    lead OTHER

Principal Investigators

  • Fritz Mattejat, PhD · Philipps University Marburg Medical Center, Dept. of Child and Adolescent Psychiatry

  • Katja J John, DP (MA) · Philipps University Marburg Medical Center, Dept. of Child and Adolescent Psychiatry

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2010-07-31
Completion
2013-07-31

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00916825 on ClinicalTrials.gov