Viewing Study NCT04662450


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Ignite Modification Date: 2026-01-17 @ 2:14 PM
Study NCT ID: NCT04662450
Status: WITHDRAWN
Last Update Posted: 2024-05-13
First Post: 2018-07-31
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Evaluation and Management of Parturients' Pain Intensity
Sponsor: Harvard Medical School (HMS and HSDM)
Organization:

Study Overview

Official Title: Evaluation and Management of Parturients' Pain Intensity
Status: WITHDRAWN
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Difficulty in recruiting patients.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed 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 Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: