Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT04662450

Evaluation and Management of Parturients' Pain Intensity

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Harvard Medical School (HMS and HSDM) · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALABM affective pain stimuliPatients undergo ABM training to shift attention away from affective pain stimuli
BEHAVIORALABM sensory pain stimuliPatients undergo ABM training to shift attention away from sensory pain stimuli
BEHAVIORALPlaceboPatients undergo ABM training to receive affective/neutral and sensory/neutral word pairs

Timeline

Start date
2024-09-01
Primary completion
2026-09-01
Completion
2026-12-01
First posted
2020-12-10
Last updated
2024-05-13

Source: ClinicalTrials.gov record NCT04662450. Inclusion in this directory is not an endorsement.