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Evaluation and Management of Parturients' Pain Intensity

H

Harvard Medical School (HMS and HSDM)

Status

Withdrawn

Conditions

Labor Pain

Treatments

Behavioral: ABM sensory pain stimuli
Behavioral: ABM affective pain stimuli
Behavioral: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT04662450
2017P001416

Details and patient eligibility

About

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.

Full 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.

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Parturients who are at 36 weeks gestation (at time of starting the study)

Exclusion criteria

  1. Any patient who refuses
  2. Patients with impaired decision-making capacity
  3. Patients who are blind or extremely visually impaired
  4. Patients who cannot understand or read English

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 3 patient groups, including a placebo group

Affective pain stimuli group
Experimental group
Description:
affective/neutral word pairs
Treatment:
Behavioral: ABM affective pain stimuli
Sensory pain stimuli group
Experimental group
Description:
sensory/neutral word pairs
Treatment:
Behavioral: ABM sensory pain stimuli
Control group
Placebo Comparator group
Description:
affective/neutral and sensory/neutral word pairs
Treatment:
Behavioral: Placebo

Trial contacts and locations

0

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Central trial contact

Jie Zhou, MD, MS, MBA

Data sourced from clinicaltrials.gov

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