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Low Back Pain Support Program During Pregnancy: A Randomized Controlled Trial

NCT05684497 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2024-11-22

No results posted yet for this study

Summary

Purpose of Research: The study was conducted as a randomized controlled experimental study to evaluate the effect of the Low Back Pain During Pregnancy Support Program (LBPSP).

Research Hypotheses H1: The perception of back pain during pregnancy in the intervention group receiving the "Low Back Pain During Pregnancy Support Program (LBPSP) will decrease compared to the control group.

H2: The Oswestry Disability Index scores of the intervention group receiving the Low Back Pain During Pregnancy Support Program (LBPSP) will decrease compared to the control group.

First interview Introductory Information Form, Low Back Pain Evaluation Form, Visual Analog Scale (VAS), and Oswestry Disability Index were applied to all pregnant women in the intervention and control groups participating in the study as pre-test at the first interview. The intervention group was conducted a LBPSP, the control group were not and were left to routine antenatal care.Four weeks after the first interview, Intervention and control groups were interviewed again, and the Low Back Pain Evaluation Form and Oswestry Disability Index scales were applied. In addition, the LBPSP Evaluation Form prepared by the researcher was applied to the pregnant women in the intervention group to evaluate the LBPSP.

Conditions

  • Low Back Pain
  • Pregnancy Related
  • Nurse's Role

Interventions

BEHAVIORAL

LBPSP in Pregnancy

LBPSP is a 50-minute interactive presentation as face to face program according to Pender's Health Promotion Model Parameters.

Sponsors & Collaborators

  • Kastamonu University

    lead OTHER

Principal Investigators

  • Münevver Aybüke Berber Çıkrık · Istanbul University Cerrahpasa Institute of Graduate Education Studies

  • Münevver Aybüke Berber Çıkrık · stanbul University Cerrahpasa Institute of Graduate Education Studies

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-07-09
Primary Completion
2022-07-30
Completion
2022-12-30

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT05684497 on ClinicalTrials.gov