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Clinical Trials/NCT02056483
NCT02056483
Completed
Not Applicable

Optimized Rehabilitation: A Randomized Study of Systematic Monitoring and Management of Breast Cancer Patients' Symptoms

Danish Cancer Society1 site in 1 country50 target enrollmentJuly 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety
Sponsor
Danish Cancer Society
Enrollment
50
Locations
1
Primary Endpoint
Psychological distress
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to examine if a psychosocial intervention including a nurse navigator and systematic symptom screening may reduce psychological and physical symptoms as well as health behavior after breast cancer.

Detailed Description

In this pilot study with a randomized controlled trial design, we examine the effect of an intervention optimizing and integrating rehabilitation for breast cancer on psychological and physical symptoms as well as health behavior after breast cancer. In the intervention group, we systematically screen for psychological and physical symptoms as well as health behavior (smoking alcohol and physical activity) not in line with the recommendations. Patients who screen positive are offered a sequence of sessions with a navigator nurse who monitor rehabilitation needs, supports the patient, educate in self-management of symptoms and refer to existing rehabilitation services as well as to up to 6 free sessions with a psychologist specialized in cancer patients. The rehabilitation services that the nurse refers to include several hospital departments and municipality services as well as general practice and by thorough follow-up on the patients use of these, the intervention aims at developing an integrated treatment and rehabilitation trajectory. The control group receives standard care.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
July 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christoffer Johansen

Professor, Head, Unit of Survivorship

Danish Cancer Society

Eligibility Criteria

Inclusion Criteria

  • diagnosis of primary breast cancer at Breast Oncology Clinic, Rigshospitalet, Copenhagen, Denmark
  • lives in Copenhagen municipality
  • score ≥7 on distress thermometer
  • able to read and understand Danish
  • not pregnant
  • expected survival more than 6 months
  • physically able to participate in rehabilitation
  • no severe psychiatric disease demanding treatment
  • no severe cognitive problems (e.g. dementia or confusion)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Psychological distress

Time Frame: 6 and 12 months

Difference in change in psychological distress between patients in the intervention and control group.Psychological distress wil be measured using the Distress Thermometer

Secondary Outcomes

  • Health related quality of life(6 and 12 months)
  • Anxiety and depression(6 and 12 months)
  • Smoking(6 and 12 months)
  • Alcohol consumption(6 and 12 months)
  • Body mass index(6 and 12 months)
  • Physical activity(6 and 12 months)
  • Use of rehabilitation services(6 and 12 months)

Study Sites (1)

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