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RECRUITING
NCT04480203
NA

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

Sponsor: Norwegian Institute of Public Health

View on ClinicalTrials.gov

Summary

1. Breast cancer patients and age-matched controls are first invited to answer questions on HRQoL. 2. Among responding breast cancer patients, a subset are invited in a randomized clinical trial with two digital interventions for cancer stress management, cognitive based stress management (CBSM) and mindfulness based intervention (MBI), as well as a control group. 3. The goal is to determine whether digital CBSM or MBI can effectively reduce stress levels as compared to a control group. Second, whether these interventions can improve HRQoL (or avoid onset of HRQoL problems) for patients with breast cancer, compared to a control group.

Official title: Coping After Breast Cancer - CABC - Stressmestring Etter Brystkreft - SEB

Key Details

Gender

FEMALE

Age Range

20 Years - 69 Years

Study Type

INTERVENTIONAL

Enrollment

390

Start Date

2021-01-15

Completion Date

2035-12-31

Last Updated

2022-03-02

Healthy Volunteers

No

Interventions

OTHER

Stressproffen cognitive based stress management

The participants will download an app (Stressproffen 2A) with cognitive based stress management.

OTHER

Stressproffen mindfulness based intervention

The participants will download an app (Stressproffen 2B) with mindfulness based intervention.

OTHER

Control

The participants will receive no app. (They will be able to download it after the end of the 3 year study).

Locations (1)

Cancer Registry of Norway

Oslo, Norway