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Rehabilitation After Breast Cancer

NCT03254875 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 309

Last updated 2021-08-27

No results posted yet for this study

Summary

The aim of the study is to evaluate whether a screening-based individually tailored nurse navigator intervention compared to standard care significantly reduce psychological and physical symptoms among women being treated for breast cancer who had moderate-to-severe distress (score ≥ 7 on the distress thermometer).

Conditions

Interventions

BEHAVIORAL

Individually tailored nurse navigation

The intervention consists of systematic report of symptoms to the nurse and up to six individual, manual-based, face-to-face or telephone nurse navigator sessions depending on individual needs.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Copenhagen University Hospital at Herlev

    collaborator OTHER

  • Danish Cancer Society

    lead OTHER

Principal Investigators

  • Pernille Bidstrup, PhD · Danish Cancer Society Research Center

  • Christoffer Johansen, DMSc · Rigshispitalet

  • Birgitte Mertz, RN · Rigshospitalet, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-15
Primary Completion
2021-03-31
Completion
2021-03-31

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

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 NCT03254875 on ClinicalTrials.gov