Coronary Artery Diseases Clinical Trial
Official title:
Clinical (Sleep, Pain and Atrial Fibrillation) and Hospital Stay Effects of Reiki and Manual Therapy After Open Heart Surgery
NCT number | NCT05853250 |
Other study ID # | 17-184 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 26, 2017 |
Est. completion date | February 5, 2020 |
Verified date | May 2023 |
Source | The Cleveland Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Reiki is an energy-based healing therapy using light touch. Manual therapy is a technique using light effleurage. These complimentary healing services are utilized to promote relaxation, sleep, improve emotions, and decrease pain; however, more research is required since sample sizes in the literature were small, subjects were generally healthy (not hospitalized), and subjects had multiple medical backgrounds. Only 1 study focused on cardiac surgery patients. We aim to learn if Reiki and manual therapy enhances postoperative clinical outcomes for patients after first time coronary artery bypass graft (CABG) and/or cardiac valve surgery. A randomized, controlled non-blinded study will enroll a sample of a minimum of 272 patient (136 per group), based on a power analysis using the primary outcome. The intervention group will receive usual care plus Reiki and manual therapy, with Reiki delivered first. Total therapies time is 20 minutes. Reiki and manual therapy will be delivered for 3 consecutive days beginning on the day after endotracheal tube removal. The usual care group will receive 20 minutes of uninterrupted rest, which is part of usual postoperative care. Outcomes are depression, anxiety, pain, night time sleep, new onset atrial fibrillation, hospital length of stay, all-cause 30-day hospital readmissions, narcotic drug burden and post-operative complications.
Status | Completed |
Enrollment | 345 |
Est. completion date | February 5, 2020 |
Est. primary completion date | September 18, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Over 18 years of age - Speaks English language and capable of reading and hearing - Up to 4 "To Come In" patients enrolled per day (2 standard care and 2 intervention group) - Arrive for surgery from outpatient (home) environment - Scheduled for surgery (arrives in "To Come In" area) on Monday and Tuesday. - Lives in one of 6 counties of North East Ohio to ensure access post-discharge hospitalization Exclusion Criteria: - History of dementia, cognitive decline, Down's syndrome or other neurologic, psychological or congenital deficiency that impacts ability to make decisions about enrollment - Severe sight and hearing impairment despite assistive devices - Cardiac surgery on a Wednesday, Thursday or Friday - Treated in the hospital prior to the day of surgery - Prolonged intubation (over 48 hours), or reinsertion of an endotracheal tube during or before the intervention is initiated (will result in intervention withdrawal) - Sedated due to new onset delirium. |
Country | Name | City | State |
---|---|---|---|
United States | Cleveland Clinic Foundation | Cleveland | Ohio |
Lead Sponsor | Collaborator |
---|---|
The Cleveland Clinic |
United States,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Depression | The Brief Symptom Inventory; 12-item survey, provides severity indexes for depression and anxiety Valid and reliable; 5-level Likert-type response set, ranging from 0, not at all to 4, extremely | Paper surveys were distributed pre-operative (baseline) | |
Primary | Depression | The Brief Symptom Inventory; 12-item survey, provides severity indexes for depression and anxiety Valid and reliable; 5-level Likert-type response set, ranging from 0, not at all to 4, extremely | Paper surveys distributed post-operative (day 3) after the final reiki and manual therapies intervention or quiet time sessions were completed. | |
Primary | Anxiety | The Brief Symptom Inventory; 12-item survey, provides severity indexes for depression and anxiety Valid and reliable; 5-level Likert-type response set, ranging from 0, not at all to 4, extremely | Paper surveys were distributed pre-operative (baseline) | |
Primary | Anxiety | The Brief Symptom Inventory; 12-item survey, provides severity indexes for depression and anxiety Valid and reliable; 5-level Likert-type response set, ranging from 0, not at all to 4, extremely | Paper surveys distributed post-operative (day 3) after the final reiki and manual therapies intervention or quiet time sessions were completed. | |
Primary | Sleep | The Richards-Campbell Sleep Questionnaire (RCSQ) Valid and Reliable; has 5 item survey as 5 domains: sleep depth, falling asleep, number of 5 items awakenings, percent of time awake, and overall quality of sleep. | Paper surveys distributed pre-operative (baseline) | |
Primary | Sleep | The Richards-Campbell Sleep Questionnaire (RCSQ) Valid and Reliable; has 5 item survey as 5 domains: sleep depth, falling asleep, number of 5 items awakenings, percent of time awake, and overall quality of sleep. | Paper surveys distributed post-operative (day 3) after final reiki and manual therapies intervention or quiet time sessions were completed. | |
Primary | Pain level | Pain intensity was assessed on a scale of 0-10 (higher score = worst pain)
• Highest (worst), lowest (least), mean and median pain scores were assessed. |
Mean (SD) value through study completion, an average of 6.4 days | |
Primary | Pain level | Pain intensity was assessed on a scale of 0-10 (higher score = worst pain)
• Highest (worst), lowest (least), mean and median pain scores were assessed. |
Mean (IQR) value through study completion, an average of 6.4 days | |
Primary | Hospital length of stay, days | Data retrieved via a hospital billing database. | Through study completion, an average of 6.4 days | |
Primary | New-onset postoperative atrial fibrillation rate (%) | Data retrieved from the Society of Thoracic Surgeons Registry | Frequency (%) of new-onset atrial fibrillation complication after open heart surgery | |
Primary | All cause 30-day hospital readmission rate, (%): | Data retrieved via a hospital billing database | 30 days after discharge | |
Primary | Total opioid IV narcotic burden (mean): | Data retrieved via a hospital billing database | Total opioid IV narcotic medication dose, using morphine equivalent data, during the length of stay, an average 6.4 days | |
Primary | Total oral narcotic burden (mean): | Data retrieved via a hospital billing database | Total oral narcotic medication dose, using morphine equivalent data, during the length of stay, an average 6.4 days |
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