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Evaluation and Management of Parturients' Pain Intensity

NCT04662450 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2024-05-13

No results posted yet for this study

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.

Conditions

  • Labor Pain

Interventions

BEHAVIORAL

ABM affective pain stimuli

Patients undergo ABM training to shift attention away from affective pain stimuli

BEHAVIORAL

ABM sensory pain stimuli

Patients undergo ABM training to shift attention away from sensory pain stimuli

BEHAVIORAL

Placebo

Patients undergo ABM training to receive affective/neutral and sensory/neutral word pairs

Sponsors & Collaborators

  • Harvard Medical School (HMS and HSDM)

    lead OTHER

Principal Investigators

  • Jie Zhou, MD, MS, MBA · Harvard Medical School (HMS and HSDM)

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-09-30
Primary Completion
2026-09-30
Completion
2026-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04662450 on ClinicalTrials.gov