Recruiting NA Breast Cancer Patients

New treatment option for Breast Cancer Patients

Official title Coping After Breast Cancer - a Randomized Clinical Trial With Two Digital Interventions

ClinicalTrials.gov ID: NCT04480203

What this study is testing

What it's testing
1. Breast cancer patients and age-matched controls are first invited to answer questions on HRQoL.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 20 to 69, women only

You may be able to join if

  • first occurrence breast cancer diagnosed from Jan 1, 2020
  • non-metastatic cancer stage 0-III Invasive tumors must be:
  • HER2 positive (regardless of ER, PR) or
  • ER negative
  • (may later include other ER+ if not conflict with recruitment for EMIT/OPTIMA)

You likely can't join if

  • None

The study team makes the final eligibility decision.

Where it's taking place

  • Oslo, Norway

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling female, 20 years to 69 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Oslo, Norway. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.