An online group cognitive behavioral psychotherapeutic program will be offered to patients with cystic fibrosis and to caregivers by the Hellenic Cystic Fibrosis Association. These 2 above therapy groups will be compared with control groups in a randomized controlled trial
Age range
18 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
SCL-90-R
Timeframe: Preintervention
SCL-90-R
Timeframe: Immediately after the intervention
SCL-90-R
Timeframe: Follow-up up to 24 weeks
SRSDA
Timeframe: Preintervention
SRSDA
Timeframe: Immediately after intervention
SRSDA
Timeframe: Follow-up up to 24 weeks
SRSDA
Timeframe: Preintervention
SRSDA
Timeframe: Immediately after intervention
SRSDA
Timeframe: Follow-up up to 24 weeks
U Uncertainty questionnaire
Timeframe: Preintervention
U Uncertainty questionnaire
Timeframe: Immediately after the intervention
U Uncertainty questionnaire
Timeframe: Follow up up to 24 weeks
Hamilton Depression Scale
Timeframe: Preintervention
Hamilton Depression Scale
Timeframe: Immediately after the intervention
Hamilton Depression Scale
Timeframe: Follow up up to 24 weeks
WHODAS total
Timeframe: Preintervention
WHODAS total
Timeframe: Immediately after the intervention
WHODAS total
Timeframe: Follow up up to 24 weeks
RAS-DS total
Timeframe: Preintervention
RAS-DS total
Timeframe: Immediately after intervention
RAS-DS total
Timeframe: Follow up up to 24 weeks