Life After Breast Cancer - Impact of a Life Coach (Lifecoach)

McGill University

Status: Unknown

Conditions: Breast Cancer; Survivorship

Treatments: Behavioral: Group life-coaching; Behavioral: Individual life-coaching

Study type: Interventional

Funder types: Other

Identifiers

NCT05020561

2022-7735

Details and patient eligibility

About

The objectives of our intervention are to

1. Ease the transition between cancer treatment and active life, and
2. Allow breast cancer survivors to take control of their lives.

The primary objective of this study is to:

1. Determine whether individual life coaching (i.e., individualized guidance that helps to put resources into action) can significantly improve quality of life and post-traumatic growth among women who have been recently treated with breast cancer.

It is hypothesized that:

1. Participants who receive both "group coaching sessions" and "individualized coaching sessions" will report greater post-traumatic growth and quality of life, and less fear of cancer recurrence when compared to the breast cancer survivors who received only the group coaching sessions or usual care.
2. Participants who receive only the group coaching sessions will report greater post-traumatic growth and quality of life, and lesser fear of cancer recurrence when compared to the participants who receive usual care.

Enrollment: 120 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. have been diagnosed with stage I, II, or III breast cancer;
2. are female breast cancer patients over the age of 18;
3. have completed anti-cancer treatment via surgery and/or chemotherapy and /or radiation therapy at the McGill University Health Centre Breast Clinic;
4. are fluent in written and spoken English or French;
5. are alert and oriented and capable of giving informed consent;
6. have an Internet connection at home that supports participation in coaching sessions via videoconferencing (zoom).

Exclusion criteria

1. have a recurrence of breast cancer;
2. are diagnosed with a second cancer;
3. are diagnosed with stage IV breast cancer due to their worse prognosis; and 4) have an active psychiatric diagnosis that would render adherence to the study problematic.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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120 participants in 3 patient groups

Arm 1 - Group and Individual

Experimental group

Description:

Participants in this experimental Arm 1 will receive the 3 group sessions followed by 4 to 5 individual coaching sessions via phone calls that last 60 minutes each.

Treatment:

Behavioral: Group life-coaching

Behavioral: Individual life-coaching

Arm 2 - Group only

Experimental group

Description:

Arm 2 will receive only the first 3 Life coach sessions (group session).

Treatment:

Behavioral: Group life-coaching

Arm 3 - Routine care

No Intervention group

Description:

Arm 3 will receive routine care by the Breast clinic team for the entire course of the study.