Cervical Cancer Clinical Trials

Find Cervical Cancer Clinical Trials Near You

Mechanisms Explaining Psychological Distress In CErvical Cancer Patients and Partners (DICE): a Population-based Prospective Study

Status: Recruiting
Location: See all (6) locations...
Study Type: Observational
SUMMARY

Objective: Gain insight into the mechanisms explaining psychological distress (i.e. anxiety, depression, cancer worry, perceived stress) in a prospective population-based sample of cervical cancer patients. Factors to be studied include characteristics of the individual (demographical and clinical, including comorbidities), characteristics of the environment ((sexual) relationships), biological function (cortisol, melatonin and sex hormone production assessed in scalp hair, inflammation and telomere length assessed in blood, overall quality of life (EORTC QLQ-C30), symptoms (EORTC QLQ-CX24), functional status (physical activity and sleep measured using the Actigraph activity tracker, and food intake measured using the online 'Eetmeter'), and general health perceptions (B-IPQ). The second aim is to assess the impact of cervical cancer on partners' distress (cancer worry, illness perceptions, relationship quality, dyadic coping).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:

• Newly diagnosed with cervical cancer stage I, II or III

• \>18 years or older

• Partner of patient participating in the study

• \>18 years

Locations
Other Locations
Netherlands
Amphia
RECRUITING
Breda
Catharina Hospital
RECRUITING
Eindhoven
University Medical Center Groningen
RECRUITING
Groningen
MUMC
RECRUITING
Maastricht
RadboudUMC
RECRUITING
Nijmegen
UMC Utrecht
RECRUITING
Utrecht
Contact Information
Primary
Nicole Ezendam, PhD
N.Ezendam@iknl.nl
+31 88 234 6096
Backup
Belle de Rooij, PhD
B.deRooij@iknl.nl
+31 88 234 6057
Time Frame
Start Date: 2020-11-01
Estimated Completion Date: 2030-01
Participants
Target number of participants: 832
Treatments
Cervical cancer patients and their partners
520 cervical cancer patients will complete questionnaires, online food diary and wear a fitbit after diagnosis, after 6 months, and after 1, 2, 5 and 10 years. In addition, a subsample (n=116) will donate blood samples and a scalp hair sample after diagnosis and 6, 12 and 24 months. We expect 312 partners of cervical cancer patients to included in the study and complete questionnaires after diagnosis, after 6 months, and after 1, 2, 5 and 10 years
Related Therapeutic Areas
Sponsors
Collaborators: Tilburg University, Netherlands Organisation for Scientific Research
Leads: Comprehensive Cancer Centre The Netherlands

This content was sourced from clinicaltrials.gov

Similar Clinical Trials