PACED-digitized Support During Adjuvant Endocrine Therapy

Sponsor
Region Stockholm (Other)
Overall Status
Recruiting
CT.gov ID
NCT05084625
Collaborator
ScientificMed Tech AB (Other), AstraZeneca (Industry), Novartis Sverige AB (Other), Bröstcancerförbundet (Other), Stockholm South General Hospital (Other), Capio St Gorans hospital (Other), Karolinska University Hospital (Other)
300
3
2
34.2
100
2.9

Study Details

Study Description

Brief Summary

The research team want to investigate whether digital support, an app under preventive hormonal breast cancer treatment can lead to less late side effects, better quality of life and increased adherence to treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: Digitized support
N/A

Detailed Description

Patients with hormon receptor positive breast cancer and adjuvant endocrine treatment will be invited to participate in the study after adjuvant radiotherapy is completed. Participants will be randomised to 12 months of access to a digital support-an app-in addition to standard follow-up or standard follow-up. Research team want to investigate whether digital support under hormonal breast cancer treatment can lead to less late side effects, better quality of life and increased adherence to treatment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
PACED-Patient-centred Digital Support During Adjuvant Endocrine Breast Cancer Treatment
Actual Study Start Date :
Oct 25, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Arm A- access to digitized support, an app

Patients in Arm A will have access to digitized support-an app for 12 months from baseline in addition to standard follow-up.

Other: Digitized support
Access to information about the disease, treatment, side effects and self-care

No Intervention: Arm B-standard follow-up

Patients in Arm B-will continue with standard follow-up from baseline and onwards

Outcome Measures

Primary Outcome Measures

  1. Difference between the two groups with regard to change in quality of life from baseline to 12 months measured by Questionnaires European Organisation for Research and Treatment for Cancer Quality of life C30 (EORTC QLQ C30). [Change from baseline to 12 months]

    EORTC QLQ C30. All of the scales and single-item measures range in score from 0 to100. A high scale score represents a higher response level. For a functional scale represents a high / healthy level of functioning, a high score for the global health status / QoL represents a high QoL, but a high score for a symptom scale / item represents a high level of symptomatology / problems. A 'little' change for better or worse on a particular scale (function or symptom) defined as changes about 5 to 10. "Moderate" change have changed about 10 to 20, and 'very much' change corresponded to a change greater than 20. Our population sample is based on that a change should be of effect size (Cohen's d) difference of 0.54 (which correspond to a moderate change) at the end of access to digital support in the primary outcome of symptom burden and quality of life, 90% power at P < .01

  2. Difference between the two groups with regard to change in quality of life from baseline to 12 months by Questionnaires European Organisation for Research and Treatment for Cancer Quality of life Breast cancerrelated 23 (EORTC QLQ BR23) [Change from baseline to 12 months]

    EORTC QLQ BR23. All of the scales and single-item measures range in score from 0 to100. A high scale score represents a higher response level. For a functional scale represents a high / healthy level of functioning, a high score for the global health status / QoL represents a high QoL, but a high score for a symptom scale / item represents a high level of symptomatology / problems. A 'little' change for better or worse on a particular scale (function or symptom) defined as changes about 5 to 10. "Moderate" change have changed about 10 to 20, and 'very much' change corresponded to a change greater than 20. BR23 recommended with C30. Our population sample is based on that a change should be of effect size (Cohen's d) difference of 0.54 (which correspond to a moderate change) at the end of access to digital support in the primary outcome of symptom burden and quality of life, 90% power at P < .01

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Hormone receptor positive breast cancer

  • On adjuvant endocrine treatment 0-16 weeks ago

Exclusion Criteria:
  • Cognitively impaired

  • No access to a mobile phone or internet

  • Not understanding Swedish

Contacts and Locations

Locations

Site City State Country Postal Code
1 Karolinska University Hospital Stockholm Sweden
2 Oncology department Capio St Gorans Hospital Stockholm Sweden
3 Södersjukhuset Stockholm Sweden

Sponsors and Collaborators

  • Region Stockholm
  • ScientificMed Tech AB
  • AstraZeneca
  • Novartis Sverige AB
  • Bröstcancerförbundet
  • Stockholm South General Hospital
  • Capio St Gorans hospital
  • Karolinska University Hospital

Investigators

  • Principal Investigator: Jenny Bergqvist, St Gorans Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Region Stockholm
ClinicalTrials.gov Identifier:
NCT05084625
Other Study ID Numbers:
  • 2021-02902
First Posted:
Oct 20, 2021
Last Update Posted:
May 12, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Region Stockholm
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2022