Self-Report Questionnaire Assessme… for Parkinson's (NCT07488351)
Testing new Parkinson treatment approach
- Trial ID
- NCT07488351
- Official Title
- "Associations of Self-Compassion and Self-Efficacy With Symptom Severity, Functional Status, and Quality of Life in Individuals With Parkinson's Disease: A Cross-Sectional Study"
- Goal
- Testing new Parkinson treatment approach
- Status
- RECRUITING
- Sponsor
- Acibadem University
- Study Type
- OBSERVATIONAL
- Enrollment
- 100 participants
- Conditions
- Parkinson Disease, Physical Disability
- Interventions
- Self-Report Questionnaire Assessment
Summary For Families
Researchers want to see whether people’s self-compassion and their confidence in managing Parkinson's relate to how severe their symptoms are, how well they function day-to-day, and their overall quality of life. Participants complete self-report questionnaires about kindness toward themselves, confidence in handling their condition, symptoms, daily function, and life quality, and researchers look for connections in those responses; no new treatment is given. The study is enrolling people aged 40 to 85 with a clinical diagnosis of Parkinson's at early to mid stages (stage 1 to 3), who can pass a short thinking and memory check (score 24 or higher), can complete the assessments and consent in writing, and do not have major depression, psychosis, advanced dementia, or other serious health problems that would affect testing.
Locations
- Acibadem University, Istanbul, Turkey, Turkey (Türkiye)
Frequently Asked Questions
- What is this trial testing?
- This trial is studying Self-Report Questionnaire Assessment. Researchers want to see whether people’s self-compassion and their confidence in managing Parkinson's relate to how severe their symptoms are, how well they function day-to-day, and their overall quality of life. Participants complete self-report questionnaires about kindness toward themselves, confidence in handling their condition, symptoms, daily function, and life quality, and researchers look for connections in those responses; no new treatment is given. The study is enrolling people aged 40 to 85 with a clinical diagnosis of Parkinson's at early to mid stages (stage 1 to 3), who can pass a short thinking and memory check (score 24 or higher), can complete the assessments and consent in writing, and do not have major depression, psychosis, advanced dementia, or other serious health problems that would affect testing.
- Who can participate?
- Participants must be between 40 Years and 85 Years.
- Where is this trial located?
- This trial is recruiting at 1 location.
- Does it cost anything to join?
- You are never charged a fee to join a legitimate clinical trial, and the study treatment and study-specific tests are provided by the trial sponsor at no charge. In the US, routine care you would receive anyway can still be billed to you or your insurance; coverage rules differ by country, and trials in the UK and Canada usually run through public health systems. Travel, parking, and time are real costs, and some trials reimburse them while others do not. Before enrolling, ask the study coordinator to explain in writing what is and is not covered.
- How long does the trial last?
- This trial is estimated to last approximately 9 months.
- Can I leave the trial if I change my mind?
- Yes. You can withdraw from any clinical trial at any time, for any reason, without affecting your standard medical care. Trials are voluntary by law. The team may ask if you are willing to do a brief exit visit so they can collect safety information, but you are not obligated.
- Can my spouse or care partner come with me to visits?
- In most cases yes, and it is often encouraged. Care partners can help with notes, questions, and getting home safely after a long visit. Some study assessments do need to happen one on one, but care partners are usually welcome for the rest of the appointment.
- Will I get a placebo in this trial?
- This is an observational study, so there is no placebo and no experimental treatment is assigned. Researchers observe and collect information while you continue your usual care.
- What procedures are involved in this trial?
- Based on the protocol, this trial involves: Questionnaires & surveys (non-invasive). Confirm the full schedule with the study coordinator.