Actively Recruiting
Evaluation of the Medical Service by Socio-aesthetics in Oncology
Led by Centre Hospitalier de Valence · Updated on 2025-09-08
400
Participants Needed
3
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of socio-aesthetics well-being care on quality of life, pain, and anxiety in patients undergoing chemotherapy for breast, prostate, colon, or lung cancer. This randomized controlled trial aims to compare socio-aesthetics care with self-administered dermo-cosmetics products during cancer treatment. The study involves 400 patients and focuses on how supportive beauty care may influence their overall well-being. Participants will be randomly assigned to one of two groups. Group A will receive four sessions of socio-aesthetics well-being care provided by qualified professionals during four consecutive chemotherapy treatments, using specific dermo-cosmetics products. Group B will self-apply the same dermo-cosmetics products without socio-aesthetics intervention across the same chemotherapy sessions. Both groups are monitored and evaluated during this period. During the study, patients will undergo 12 assessments between the second and fifth chemotherapy cycles to measure pain with the EVA scale, anxiety with the HADS questionnaire, and the impact of socio-aesthetics care using the Patient Centricity Questionnaire (PCQ). Data will be collected electronically, and participants will be followed for three months after enrollment. The study aims to capture the influence of socio-aesthetics care on patient-reported quality of life, pain, and anxiety over this timeframe.
CONDITIONS
Brief Title
Evaluation of the Medical Service by Socio-aesthetics in Oncology
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 18 years old
- Currently treated with chemotherapy for lung, breast, colon, or prostate cancer
- Able to understand, read, and write French
- Affiliated with a social security scheme
- Dated and signed informed consent provided
You will not qualify if you...
- Unable to be followed for medical, social, family, geographic, or psychological reasons for the study duration
- Deprived of liberty by court or administrative decision
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Duration of 4 consecutive chemotherapy administrations
Participants receive either 4 sessions of socio-aesthetics well-being care performed by a qualified person or self-administer dermo-cosmetic products themselves during 4 consecutive chemotherapy administrations.
4 visits coinciding with chemotherapy administrations
Duration - 3 months
Participants are followed for 3 months to assess quality of life, pain, and anxiety.
12 evaluations between chemotherapy cure 2 and chemotherapy cure 5
Trial Site Locations
Total: 3 locations
1
Centre Antoine Lacassagne
Nice, France
Actively Recruiting
2
AP HP
Paris, France
Actively Recruiting
3
Chru Tours
Tours, France
Actively Recruiting
Research Team
G
Guillaume Guillaume, PHD
S
sandrine Beauchard
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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