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Evaluation and Management of Parturients' Pain Intensity

Labor Pain Clinical Trial

Official title:
Evaluation and Management of Parturients' Pain Intensity

Clinical Trial Summary

The primary objective of this study is to examine the effects of Attentional Bias Modification (ABM) on the labor pain in parturients. One-third of the participants will undergo ABM training away from affective pain stimuli. One-third of the participants will undergo ABM training away from sensory pain stimuli. The rest of participants will be the control group.

Clinical Trial Description

In recent years, significant attention has been paid to the attentional bias in patients with chronic pain. Studies found that Attentional Bias Modification (ABM) could reduce the pain intensity in participants with chronic pain. The investigator's goal is to evaluate the effects of ABM on labor pain and patient satisfaction with the labor and delivery experience. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04662450
Study type Interventional
Source Harvard Medical School (HMS and HSDM)
Contact
Status Withdrawn
Phase N/A
Start date September 2024
Completion date December 2026
View Details
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