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No resources available to carry out the trial.
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| Name | Class |
|---|---|
| Thimble Health | UNKNOWN |
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The goal of this clinical trial is to lessen the pain and fear of needles by using a mindfulness-based app and a recovery patch on pediatric patients between the ages of 5 and 11. The main questions it aims to answer are:
Participants will be asked to be part of a clinical trial in which they will be picked to be in one of four groups: control (no use of the patch or app), use of Thimble Mindfulness App only (Experimental- App), use of Thimble Recovery Patch only (Experimental-Patch), or use of both Thimble Mindfulness App and Recovery Patch (Experimental-Patch and App). Patients will be asked to:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | No application and no thimble patch. | |
| Use of the thimble application but not the thimble patch | Experimental | Use of the thimble application but not the thimble patch |
|
| Use of the thimble patch but not the thimble application | Experimental | Use of the thimble patch but not the thimble application |
|
| Use of both thimble application and thimble patch | Experimental | Use of both thimble application and thimble patch |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Thimble Application | Device | Use of of thimble application to practice mindfulness before needle procedure. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Scores from the State Trait Anxiety Inventory for Children (STAI-C) | Measures anxiety in children. Children respond to the STAI-C by selecting one of three choices for each item that best represents how they feel. Each STAI-C item is measured on a 3-point rating scale for which each response is assigned values of either 1, 2, or 3. Scores on the STAI-C range from a minimum of 20 to a maximum of 60. Higher scores indicate greater levels of anxiety. | Measured upon enrollment, immediately before needle-based procedure, immediately after needle-based procedure and 24-48 hours after procedure |
| Measure | Description | Time Frame |
|---|---|---|
| Perceived Swelling | Patients and/or parents will describe whether or not they felt the patch helped provide some relief from swelling in feedback survey | 24-48 hours after needle-based procedure |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bianca Edison, MD | Children's Hospital Los Angeles | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Children's Hospital Los Angeles | Los Angeles | California | 90027 | United States |
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| ID | Term |
|---|---|
| C000719205 | Iatrophobia |
| D000088823 | Vaccination Hesitancy |
| ID | Term |
|---|---|
| D000072758 | Vaccination Refusal |
| D016312 | Treatment Refusal |
| D000074822 | Treatment Adherence and Compliance |
| D015438 | Health Behavior |
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One control group and three intervention groups.
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| D001519 | Behavior |