Anxiety Clinical Trial
— Dixon ProjectOfficial title:
The Effect of Touch on Pain and Anxiety During the Bone Marrow Biopsy Procedure
NCT number | NCT04935775 |
Other study ID # | D21039 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 13, 2021 |
Est. completion date | April 20, 2022 |
Verified date | June 2023 |
Source | Dartmouth-Hitchcock Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is analyzing the benefit of untrained touch provided during a bone marrow biopsy procedure as compared to performing the procedure without providing it.
Status | Completed |
Enrollment | 46 |
Est. completion date | April 20, 2022 |
Est. primary completion date | January 28, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Patients from Norris Cotton Cancer Center who have been scheduled for a bone marrow biopsy at the Outpatient Surgical Center at Dartmouth-Hitchcock Medical Center. 2. Subjects must be able to read and write in English to provide informed consent and fill out the questionnaires. Exclusion Criteria: 1. Patients who do not wish to have their feet and lower legs touched during the procedure 2. Open sores on their feet or lower legs. |
Country | Name | City | State |
---|---|---|---|
United States | Dartmouth Hitchcock Medical Center, Dartmouth Cancer Center | Lebanon | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
Dartmouth-Hitchcock Medical Center |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluate patient-reported pain levels | Patients be asked to describe what their pain level was before, at its worst point during the procedure and after the bone marrow biopsy. The Visual Analog Scale (VAS) will be used on a 0 to 10 scale, 0 being no pain at all and 10 being the worst pain imaginable. | During the study procedure | |
Primary | Evaluate patient-reported anxiety levels | The six -item short form Spiellberger State-Trait Anxiety Inventory (STAI), a self-reported questionnaire, will be administered on pencil and paper. Possible ranges of scores on the 6-item questionnaires vary from 6 to 24, with separate scores for both the state and trait anxiety sections. Answers to each question range from 1 to 4, 1 being no anxiety at all to 4 being very high anxiety (Julian, 2014). Patients will complete the short-form STAI before and after the procedure. | During the study procedure | |
Primary | Identify correlation between demographics and interventional response | Secondary endpoints will include identifying any correlation between demographic data collected and response to the intervention. The patient experience will be evaluated by using a visual analog scale at the completion of the procedure via paper and pencil that the subjects will complete independently. These open ended questions will be used to inform larger study questions in the future. Abstracted and deidentified summaries of responses will be prepared by the study PI. | During the study procedure |
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