Online and in-person support for anxiety and depression in cancer caregivers
Impact of Online or In-person Cognitive Behavioural Psychotherapy Interventions on Anxiety and Depression Symptoms in Caregivers of Patients with Cancer
This study is testing whether online or in-person therapy can help caregivers of cancer patients who are feeling anxious or depressed.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Fondazione ANT Italia ONLUS Academic / other |
| Locations | 1 site (Bologna, BO) |
| Trial ID | NCT06592573 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of online and in-person Cognitive Behavioral Therapy (CBT) interventions for caregivers of cancer patients who experience anxiety and depressive symptoms. Caregivers, who often face significant emotional challenges, will receive psychological support tailored to their needs, either through telemedicine or face-to-face sessions. The study will assess the impact of these interventions on the caregivers' mental health, utilizing standardized scales to measure anxiety and depression levels. By comparing the outcomes of both intervention methods, the study seeks to determine the most effective approach for providing psychological support.
Who should consider this trial
Good fit: Ideal candidates for this study are caregivers of cancer patients aged 18 and older who exhibit symptoms of anxiety and depression.
Not a fit: Patients with severe psychiatric conditions or cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve the mental health and quality of life for caregivers of cancer patients.
How similar studies have performed: Previous studies have shown that web-based psychological interventions can effectively reduce anxiety and depression symptoms, indicating a promising approach for this population.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Presence of anxious-depressive symptomatology, included in the cut-off 5-21 of the Generalized Anxiety Disorder Scale-7 (GAD-7) and/or in the cut-off 5-27 of the Patient Health Questionnaire-9 (PHQ-9). * Aged 18 years or older. * Able to understand the aims of the study and to sign the informed consent. * Able to understand the Italian language. * Able to use a technological tool for tele-consultations (smartphone, tablet, computer, etc.). Exclusion Criteria: * With severe psychiatric pathology causing clinically significant impairment of functioning in social, occupational or other important areas. * With cognitive impairment. * Engaged in psychological support/psychotherapy within the last 3 months. * Who does not meet the inclusion criteria.
Where this trial is running
Bologna, BO
- Fondazione ANT — Bologna, Bo, Italy (Recruiting)
Study contacts
- Principal investigator: Silvia Varani — Fondazione ANT Italia ONLUS
- Study coordinator: Rita Ostan, PhD
- Email: rita.ostan@ant.it
- Phone: +390517190153
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.