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Optimized Rehabilitation Following Primary Breast Cancer Surgery

NCT03434717 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 643

Last updated 2023-12-14

No results posted yet for this study

Summary

This study aims to evaluate the effects of an intervention based on systematic screening of psychological distress as the basis for individualised support and rehabilitation following primary breast cancer surgery focusing on psychological , physical and health-economics outcomes. The aim is also to illuminate patients' and relatives' experiences and need of support during the rehabilitation .

Conditions

  • Rehabilitation
  • Breast Neoplasms
  • Psychological Distress

Interventions

OTHER

Individualised rehabilitation

Patients will get access/support to individualised rehabilitation based on their needs identified through the distress thermometer

OTHER

Care as usual

Patients will get care as usual

Sponsors & Collaborators

  • Lund University

    lead OTHER

Principal Investigators

  • Marlene Malmström, PhD · Lund university, department of health siences, Lund

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-15
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • Sweden

Study Locations

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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 NCT03434717 on ClinicalTrials.gov