Actively Recruiting
e-Motion : Promoting Emotion Regulation in Chronic Cancer
Led by Université Libre de Bruxelles · Updated on 2025-11-21
30
Participants Needed
2
Research Sites
58 weeks
Total Duration
On this page
Sponsors
U
Université Libre de Bruxelles
Lead Sponsor
C
Centre de Psycho-Oncologie (CPO)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The present study aimed to pilot evaluate two interventions: a Guided Self-Help Intervention alone, and a combined Group and Guided Self-Help Intervention, designed to support individuals living with chronic cancer and recently diagnosed. The primary aim of this pilot study is to assess the feasibility, acceptability and tolerability of the interventions. The secondary aim of the pilot study is to assess the interventions preliminary efficacy and differences on psychological symptoms.
CONDITIONS
Official Title
e-Motion : Promoting Emotion Regulation in Chronic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with chronic cancer (various metastatic types or symptomatic multiple myeloma) within the past 12 months
- Completed at least one active cancer treatment such as chemotherapy, surgery, radiotherapy, immunotherapy, or targeted therapy
You will not qualify if you...
- Life expectancy less than one year
- More than specified treatment lines based on cancer type (e.g., more than one for triple negative breast cancer; more than three for prostate cancer and multiple myeloma)
- Diagnosis of oligometastatic cancer
- Under 18 years old
- Not fluent in French
- Unable to follow an online intervention
- Severe cognitive impairment or severe/acute psychiatric disorder
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Institut Jules Bordet, Hôpital universitaire de Bruxelles
Brussels, Anderlecht, Belgium, 1070
Not Yet Recruiting
2
H.U.B Institut Jules Bordet
Brussels, Brussels Capital, Belgium, 1070
Actively Recruiting
Research Team
F
Florence Lewis, PhD
CONTACT
I
Isabelle Merckaert, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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