Reiki Effects on Bone Marrow Transplant Patients (NCT05694910) | Clinical Trial Compass
UnknownNot Applicable
Reiki Effects on Bone Marrow Transplant Patients
Turkey (Türkiye)42 participantsStarted 2022-08-01
Plain-language summary
The aim of the study is to examine the effect of Reiki on fatigue, vital signs, and engraftment in bone marrow transplant patients.
Who can participate
Age range
18 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:
* Being over 18 years old
* Not having a communication problem,
* Autologous bone marrow transplantation has been performed
* Willingness to participate in Reiki practice,
* To be competent to answer the data collection tools to be used in the research.
* Not using complementary practices (energy therapies) in the last six months.
Exclusion Criteria:
* Having a communication problem
* Application of allogeneic bone marrow transplantation
* Not being willing to engage in Reiki practice
* Reiki practitioner or instructor,
* Have received energy therapy sessions such as Reiki/Therapeutic touch/Healing touch in the last six months
* Application of bone marrow transplantation for hematological cancers
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
Personal Information Form
Timeframe: Baseline
2
Visual Analog Scale
Timeframe: Change from baseline Visual Analog Scale at one week
3
Fatigue
Timeframe: Change from fatigue level at a week
4
Engraftment
Timeframe: After one week
5
Change from Leukocyte values at a week
Timeframe: Change from Leukocyte values at a week
6
Change from Hemoglobin values at a week
Timeframe: Change from Hemoglobin values at a week
7
Change from Hematocrit values at a week
Timeframe: Change from Hematocrit values at a week