Evaluation of Psychotherapeutic Intervention Model in Nursing (NCT06076746) | Clinical Trial Compass
CompletedNot Applicable
Evaluation of Psychotherapeutic Intervention Model in Nursing
Turkey (Türkiye)20 participantsStarted 2024-10-14
Plain-language summary
This study aims to evaluate the efficacy of a psychotherapeutic intervention model in nursing on the nursing diagnosis ineffective coping. For this purpose, validity and reliability studies of the assessment tools will be carried out initially, and then a randomized controlled study will be conducted.
Who can participate
Age range
18 Years – 64 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.
Inclusion Criteria:
* 18-64 years old,
* Literacy,
* Having applied to the psychiatry outpatient clinic,
* Being regularly treated in a psychiatry outpatient clinic,
* Having a medical diagnosis of generalized anxiety disorder,
* Having at least one of the defining characteristics of the nursing diagnosis of ineffective coping according to the nursing process.
Exclusion Criteria:
* Medical diagnosis of dementia or psychotic spectrum disorder,
* Cognitive disorder,
* Confused state of consciousness
* Psychomotor agitation,
* Moderate or severe intellectual disability
* Expressing suicidal thoughts
* Suicide attempt in the last month
* Continuing psychological counseling at the moment.
Questions worth asking your doctor
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.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
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.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Coping
Timeframe: Baseline and through study completion, an average of 9 weeks
2
Self esteem
Timeframe: Baseline and through study completion, an average of 9 weeks