Chronic Cancer Pain Management Program (ICMP)

Hamilton Health Sciences (HHS)

Status: Enrolling

Conditions: Breast Cancer; Pain Cancer; Cancer, Treatment-Related

Treatments: Behavioral: I-Can-Manage-Pain after cancer (Pain Management Program)

Study type: Interventional

Funder types: Other

Identifiers

NCT06101849

16187

Details and patient eligibility

About

The goal of this research study is to evaluate an online inter-professional pain management program for survivors of breast cancer.

The main questions it aims to answer:

1. whether this treatment will help address the pain management concerns of patients,
2. whether it is feasible to offer this treatment in the future as multi-centre randomized controlled trial (RCT).

Participants will be asked to attend a 6-week online pain management group sessions (1h/week). Participants will also be asked to fill out questionnaires before and after the program completion.

Full description

Survivors of breast cancer often experience chronic pain that is undertreated and gets in the way of their functioning, relationships, mental health, and quality of life. There is little research on the best ways of treating chronic pain in cancer that make good use of all the expertise offered by different health care providers such as nurses, psychologists, and physiotherapists. In addition, little is known about how to offer such a service in an online format.

This study aims to pilot an online interprofessional pain management program for survivors of breast cancer. The investigators would like to know whether this treatment will help address the pain management concerns of patients, and whether it is feasible to offer this treatment in the future as multi-centre randomized controlled trial (RCT).

Participants in the study will attend a 6-week online pain management program (I-Can-Manage-Pain after cancer) that will cover the topics of understanding cancer pain, exercises to manage pain and psychological strategies to cope with pain. Questionnaires will be administered before and after the program to assess their satisfaction and changes in outcomes related to pain, quality of life, confidence to manage their pain, and use of health care services. The feasibility of implementing the study and the program will be pre-determined by an acceptability criteria for patient recruitment, completion of questionnaires, participation in the online sessions, and satisfaction with the pain management program.

It is hoped that study findings will help inform the development of treatment programs to improve post-treatment pain management and the quality of life of survivors of breast cancer patients.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. diagnosis of Stage 1-3 breast cancer;
2. had surgical excision at least 3 months ago;
3. completed neoadjuvant/adjuvant chemotherapy and/or radiation treatment at least 4 months ago;
4. within 5 years post active cancer treatment;
5. persistent pain within the last 3 months that is bothersome;
6. medical clearance to participate in the intervention
7. over 18 years of age;
8. verbal fluency in English;
9. have access to internet and technology to participate in the online program. Patients currently receiving adjuvant endocrine therapy or molecularly targeted therapies or who have completed these therapies within the last 5 years are eligible to participate.

Exclusion criteria

• Participants will be excluded from the study if they:

  1. demonstrate significant cognitive impairment as determined by the clinical judgment of the provider;
  2. have a pre-existing non-cancer pain condition,
  3. have severe emotional distress that interferes with group participation as determined by scores above 15 on the Patient Health Questionnaire-9.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

Cancer Pain Management Group

Experimental group

Description:

Participants in the study will attend a 6-week online pain management program (I-Can-Manage-Pain after cancer) that will cover the topics of understanding cancer pain, exercises to manage pain and psychological strategies to cope with pain. Questionnaires will be administered before and after the program

Treatment:

Behavioral: I-Can-Manage-Pain after cancer (Pain Management Program)