Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05887102

Pilot Study of PACHA Program to Enhance Adherence to Adjuvant Endocrine Therapy Among Breast Cancer Survivors

Led by CHU de Quebec-Universite Laval · Updated on 2024-08-22

66

Participants Needed

1

Research Sites

90 weeks

Total Duration

On this page

Sponsors

C

CHU de Quebec-Universite Laval

Lead Sponsor

C

Canadian Institutes of Health Research (CIHR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this randomized controlled pilot study is to assess the feasibility, acceptability, and preliminary effects of the PACHA program designed for women having an adjuvant endocrine therapy (AET) after hormone-sensitive breast cancer. PACHA (programme en Pharmacie pour l'ACcompagnement des femmes ayant de l'Hormonothérapie Adjuvante) is a community pharmacy-based program aimed at optimizing the experience of AET and its use. The main questions it aims to answer are : * Does the program have an effect on factors expected to influence AET adherence? * Is the program acceptable? * Is the implementation of the program feasible? * What is the feasibility of procedures for carrying out a full-scale study? Participating community pharmacies will be randomized. Pharmacists working in pharmacies assigned to the PACHA group (33 pharmacies) will receive web-based training and manuals to use during their consultations with women having an AET. Recruited women attending these pharmacies will also have access to information and resources about AET (videos, evidence-based booklet). Pharmacists practicing in pharmacies assigned to the control group (33 pharmacies) will provide usual care.

CONDITIONS

Official Title

Pilot Study of PACHA Program to Enhance Adherence to Adjuvant Endocrine Therapy Among Breast Cancer Survivors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pharmacy is located in the province of Quebec, Canada
  • At least one pharmacist agrees to manage the project in the pharmacy
  • At least one woman has started adjuvant endocrine therapy (AET) in the last 6 months at the pharmacy
  • Pharmacist practices in a Quebec pharmacy
  • Pharmacist provides consent to participate
  • Women are 18 years or older
  • Women diagnosed with first non-metastatic, hormone-sensitive breast cancer
  • Women received AET prescription for the first time within last 6 months
  • Women are fluent in French
  • Women have internet access
  • Women provide consent to participate
Not Eligible

You will not qualify if you...

  • Women living in residential facilities where AET medication is not self-managed

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Trial Site Locations

Total: 1 location

1

Centre de recherche du CHU de Québec

Québec, Quebec, Canada, G1S 4L8

Actively Recruiting

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Research Team

S

Sophie Lauzier, Ph.D.

CONTACT

J

Julie Lapointe, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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