Anchoring Patients Pain Scores in the Emergency Department
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04717518 |
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Recruitment Status :
Recruiting
First Posted : January 22, 2021
Last Update Posted : January 22, 2021
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| Condition or disease | Intervention/treatment |
|---|---|
| Abdominal Pain Chest Pain Headache Joint Pain Muscle Pain Back Pain Neck Pain | Other: Measurement of Pain |
| Study Type : | Observational |
| Estimated Enrollment : | 1000 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Anchoring Patients Pain Scores in the Emergency Department |
| Actual Study Start Date : | August 24, 2020 |
| Estimated Primary Completion Date : | August 2022 |
| Estimated Study Completion Date : | August 2022 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Lower Anchor Survey
Patients will likely rate their pain lower.
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Other: Measurement of Pain
Patients will fill out a brief survey concerning the current visit to the ED. |
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Higher Anchor Survey
Patients will likely rate their pain higher.
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Other: Measurement of Pain
Patients will fill out a brief survey concerning the current visit to the ED. |
- Utilization of a questionnaire to measure the mean pain scores between two intervention groups based on the numeric pain score scale [ Time Frame: Through study completion, an average of 1 year ]A questionnaire will be used to measure pain scores by utilizing a numeric pain scale (0-100) and measure the effect of anchoring bias on pain scores in the Emergency Department. It is hypothesized that a lower pain score anchor will lead to a lower reported pain score by the patient.
- An analysis to examine the influence of anchoring on patient satisfaction for patients with common chief complaints related to pain in the Emergency Department. It is unknown if anchoring affects a patient's overall satisfaction. [ Time Frame: Through study completion, an average of 1 year ]Patients receive Press-Ganey questionnaire to evaluate their visit to the Emergency Department. We will measure if the anchoring pain score affects the patients overall satisfaction with their Emergency Department care.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- 18 years of age or older
- Presenting to the ED with a chief complaint of any type of pain
Exclusion Criteria:
- Under 18 years of age
- Refusal to consent
- Incarcerated patients
- Pregnant patients
- Unable to complete survey secondary to clinical instability, severe pain, or disorientation determined by a study physician
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04717518
| Contact: Lynn Carrasco | 361-861-1865 | lynn.carrasco@christushealth.org | |
| Contact: Peter Richman, MD | 361-861-1872 | prichmanmdmba@gmail.com |
| United States, Texas | |
| CHRISTUS Spohn Health System | Recruiting |
| Corpus Christi, Texas, United States, 78404 | |
| Contact: Landry Dorsett, DO 361-861-1865 landrydorsett@gmail.com | |
| Contact: Peter Richman, MD 361-861-1872 prichmanmdmba@gmail.com | |
| Principal Investigator: Landry Dorsett, DO | |
| Sub-Investigator: Peter Richman, MD | |
| Principal Investigator: | Landry Dorsett, DO | CHRISTUS Spohn Health System |
| Responsible Party: | Landry Dorsett, DO, Principal Investigator, CHRISTUS Health |
| ClinicalTrials.gov Identifier: | NCT04717518 |
| Other Study ID Numbers: |
2020-132 |
| First Posted: | January 22, 2021 Key Record Dates |
| Last Update Posted: | January 22, 2021 |
| Last Verified: | January 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | Plans to collaborate with other universities in other studies and/or grants. |
| Supporting Materials: |
Study Protocol Statistical Analysis Plan (SAP) Clinical Study Report (CSR) |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Emergency Room |
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Arthralgia Myalgia Emergencies Headache Neck Pain Chest Pain Abdominal Pain Pain Neurologic Manifestations |
Disease Attributes Pathologic Processes Signs and Symptoms, Digestive Joint Diseases Musculoskeletal Diseases Muscular Diseases Neuromuscular Diseases Nervous System Diseases Musculoskeletal Pain |

