Sexual Function, Body Image, Kinesiophobia and Physical Activity in Pregnant Women

Sponsor
Muş Alparlan University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05990361
Collaborator
(none)
118
1
4.2
28.1

Study Details

Study Description

Brief Summary

This study compares sexual function, body image, kinesiophobia and physical activity level in women with and without pregnancy-related pelvic girdle pain.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: clinical diagnostic test

Detailed Description

Pelvic girdle pain (PGP) is a condition felt around the posterior iliac crystals, gluteal region and the sacroiliac joints, may spread to the back of the thigh, and may occur together or separately with pain in the symphysis pubis. Pregnancy-related PGP causes problems in the sexual life of women. Body image differs with the development of physical symptoms and changes in body size and shape during pregnancy. Body dissatisfaction resulting from physical changes can cause problems in women's attitudes towards sexuality. Sexual function is affected by physiological, anatomical and psychological changes that occur during pregnancy. Sexual function during pregnancy has been associated with conditions such as body image, physical activity level, and pain.

In the literature, there are studies evaluating the relationship between sexual function and body image in pregnant women and in different populations. However, in these studies, questionnaires specific to pregnant women were not used to evaluate sexual function and body image, and a comparison of these parameters was not investigate in women with and without pregnancy-related PGP.

Therefore, this study was planned to compare sexual function, body image, kinesiophobia and physical activity levels in women with and without pregnancy-related PGP.

The outcome measures are Pregnancy Sexual Response Inventory (PSRI), Body Image in Pregnancy Scale (BIPS-Turkish), Tampa Kinesiophobia Scale (TKS) and Pregnancy physical activity questionnaire (PPAQ).

The clinical diagnosis tests are Active Straight Leg Rise, Posterior Pelvic Pain Provocation Test, Long Dorsal Sacroiliac Ligament Palpation, Pelvic Compression, Pelvic Distraction, Patrick-Faber Test and Gaenslen Test.

Study Design

Study Type:
Observational
Anticipated Enrollment :
118 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Comparison of Sexual Function, Body Image, Kinesiophobia and Physical Activity Level in Women With and Without Pregnancy-related Pelvic Girdle Pain''
Actual Study Start Date :
Apr 24, 2023
Anticipated Primary Completion Date :
Aug 30, 2023
Anticipated Study Completion Date :
Aug 30, 2023

Arms and Interventions

Arm Intervention/Treatment
women with pelvic girdle pain

The subjects who have at least one positive result from Active Straight Leg Raise, and Posterior Pelvic Pain Provocation Tests; and at least two positive results from the Pelvic Compression and Distraction, Patrick Faber, Gaenslen and Long Dorsal Sacroiliac Ligament Palpation tests are classified as with PGP group.

Diagnostic Test: clinical diagnostic test
The clinical diagnosis tests are Active Straight Leg Rise ASLR, Posterior Pelvic Pain Provocation, Long Dorsal Sacroiliac Ligament Palpation (LDSLP), Pelvic Compression, Pelvic Distraction, Patrick-Faber Test (PF), and Gaenslen Test (GT). The subjects who had at least one positive result from ASLR and P4 Tests; and at least two positive results from the Pelvic Compression and Distraction, PF, GT and LDSLP tests are classified as with PGP group.

women without pelvic girdle pain

The subjects who have not at least one positive result from Active Straight Leg Raise, and Posterior Pelvic Pain Provocation Tests; and at least two positive results from the Pelvic Compression and Distraction, Patrick Faber, Gaenslen and Long Dorsal Sacroiliac Ligament Palpation tests are classified as without PGP group.

Diagnostic Test: clinical diagnostic test
The clinical diagnosis tests are Active Straight Leg Rise ASLR, Posterior Pelvic Pain Provocation, Long Dorsal Sacroiliac Ligament Palpation (LDSLP), Pelvic Compression, Pelvic Distraction, Patrick-Faber Test (PF), and Gaenslen Test (GT). The subjects who had at least one positive result from ASLR and P4 Tests; and at least two positive results from the Pelvic Compression and Distraction, PF, GT and LDSLP tests are classified as with PGP group.

Outcome Measures

Primary Outcome Measures

  1. Pregnancy Sexual Response Inventory-Turkish version [immediately before the clinical diagnostic tests will be applied the questionnaire]

    to assess sexual functions in pregnant women with and without PGP

  2. Body Image in Pregnancy Scale (BIPS-Turkish) [immediately before the clinical diagnostic tests will be applied the questionnaire]

    to evaluate body image perceptions of Turkish pregnant women with and without PGP

  3. Tampa Scale for Kinesiophobia-Turkish version [immediately before the clinical diagnostic tests will be applied the questionnaire]

    to evaluate level of kinesiophobia of Turkish pregnant women with and without PGP

  4. Pregnancy Physical Activity Questionnaire-Turkish version [immediately before the clinical diagnostic tests will be applied the questionnaire]

    To evaluate the physical activity level of pregnant women with and without PGP

Secondary Outcome Measures

  1. Pelvic Girdle Questionnaire Pelvic Girdle Questionnaire-Turkish version [immediately after the clinical diagnostic tests for PGP will be applied the questionnaire]

    To evaluate both disability and symptoms women with pregnancy-related PGP

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being between 18 and 40 years-old,

  • Being second or third trimester of pregnancy

  • Being literate in Turkish

Exclusion Criteria:
  • Having a pregnancy complication (preeclampsia, pregnancy-induced hypertension, diabetes, etc.),

  • Having a known gynecological or urological problem that may mimic PGP

  • Having neurological (multiple sclerosis, spinal cord injury, etc.), orthopedic (hip dislocation, etc.), cardiopulmonary (heart failure, chronic obstructive pulmonary disease, etc.) problems that affect sexual function and physical activity,

  • Having situations in which sexual activity is contraindicated and should be restricted (placenta previa, risk of premature birth, cervical insufficiency, antepartum hemorrhage, premature rupture of membranes, genital infection, etc.),

  • Having visual, auditory and cognitive problems that may prevent participation in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Semiha Yenişehir Muş Turkey 49000

Sponsors and Collaborators

  • Muş Alparlan University

Investigators

  • Principal Investigator: SEMİHA YENİŞEHİR, Muş Alparslan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Muş Alparlan University
ClinicalTrials.gov Identifier:
NCT05990361
Other Study ID Numbers:
  • 18.04.2023-90204
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Muş Alparlan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 14, 2023