Comparison of Two Abdominal Exercise Programs on the Interrect Distance

Sponsor
University of Vigo (Other)
Overall Status
Recruiting
CT.gov ID
NCT05439668
Collaborator
(none)
20
1
2
7.1
2.8

Study Details

Study Description

Brief Summary

The objective of the research is to compare two programs of exercises in postpartum woman, one based in abdominal strengthening exercises and the other based in abdominal hypopresive exercise.

Condition or Disease Intervention/Treatment Phase
  • Other: Classic abdominal strengthening exercises
  • Other: Hypopressive abdominal exercises program
N/A

Detailed Description

Diastasis recti abdominisis the separation of the two rectus abdominis muscles along the linea alba with a consequent separation of fibres and widening of the same. The linea alba has different functions which include supporting the proximal anterior recti, guaranteeing the stability of the vertebral column, pelvis and the pelvic floor, and intervening in the function of the abdominal muscles since it serves as their anterior anchorage.

The crunch abdominal exercise (classic abdominal) is the most studied exercise used to test the behaviour of the linea alba, and in most cases, a decrease in the inter-rectus distance is observed when compared to the resting stage. In the oder hand, Abdominal hypopresives exercises were designed for women in the postpartum period but the effects over the abdominal muscles is unknown and the authors are unaware of any study that evaluates the effect of a hypopressive exercise program on the interrectus distance.

The objective of the research is to compare two programs of exercises in postpartum woman, one based in abdominal strengthening exercises and the other based in abdominal hypopresive exercise.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of Two Abdominal Exercise Programs on the Interrect Distance in Postpartum Woman
Actual Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Oct 10, 2022
Anticipated Study Completion Date :
Dec 3, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Classic abdominal exercises Group

This group will carry out an abdominal strengthening exercise program based on the classic abdominal exercises.

Other: Classic abdominal strengthening exercises
Classic abdominal strengthening exercises (Curl-up, sit-ups and leg-rise), balance exercises, general mobility and upper limb strengthening exercises.

Experimental: Abdominal hypopresives exercise Group

This group will carry out an abdominal strengthening exercise program based on the abdominal hypopressives exercises.

Other: Hypopressive abdominal exercises program
Hypopressive abdominal exercises, balance exercises, general mobility and upper limb strengthening exercises

Outcome Measures

Primary Outcome Measures

  1. Interrectus distance measure [Baseline, preintervention]

    he participants will be placed in supine decubitus with the knees flexed to 90º with the feet resting on the stretcher and the arms along the body. After receiving the instructions to perform an abdominal crunch, subjects are asked to lift their heads and lift shoulders until the scapula lifts off the table. The ultrasound images will be recorded with an ultrasound scanner (GE Logic and; 4 12MHz, 39mm linear transducer; mode B), in a position of supine rest and a position of muscle activation (isometric contraction), 2 cm and 5 cm above the navel. Centimeters are the unit of measurement.

  2. Interrectus distance measure [After the intervention]

    he participants will be placed in supine decubitus with the knees flexed to 90º with the feet resting on the stretcher and the arms along the body. After receiving the instructions to perform an abdominal crunch, subjects are asked to lift their heads and lift shoulders until the scapula lifts off the table. The ultrasound images will be recorded with an ultrasound scanner (GE Logic and; 4 12MHz, 39mm linear transducer; mode B), in a position of supine rest and a position of muscle activation (isometric contraction), 2 cm and 5 cm above the navel. Centimeters are the unit of this measurement.

Secondary Outcome Measures

  1. Maternal age [Preintervention]

    Age when the woman gave birth. This variable will be managed by the midwives through their clinical history. Years are the unit of this measurement.

  2. Fetal weight [Preintervenrion]

    Weight baby This variable will be managed by the midwives through their clinical history. Kilogrames are the unit of this measurement.

  3. Number of deliveries [Preintervention]

    Total of number of deliveries. This variable will be managed by the midwives through their clinical history. Absolut number are the unit of this measurement.

  4. Weight gain during pregnancy [Preintervention]

    Weight gain during pregnancy. This variable will be managed by the midwives through their clinical history. Kilogrames are the unit of this measurement.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Women having given birth 8 weeks before starting the study treatment

  • Women agree to participate in the study

  • Women with vaginal delivery.

Exclusion Criteria:
  • Women with abdominal hernia

  • Pregnancy woman

  • Previus Abdominal Surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 Iria Da Cuña Carrera Pontevedra Spain 36005

Sponsors and Collaborators

  • University of Vigo

Investigators

  • Principal Investigator: Iria Da Cuña-carrera, PHD, Universitu of Vigo

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Iria Da Cuña Carrera, Principal investigator, University of Vigo
ClinicalTrials.gov Identifier:
NCT05439668
Other Study ID Numbers:
  • 17062022
First Posted:
Jun 30, 2022
Last Update Posted:
Jun 30, 2022
Last Verified:
Jun 1, 2022
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 Iria Da Cuña Carrera, Principal investigator, University of Vigo

Study Results

No Results Posted as of Jun 30, 2022