An interventional study of Multimodal Physiotherapy Exercise Programme in Pelvic Floor, sponsored by Universidad Miguel Hernandez de Elche. Completed. Open to female participants aged 18 Years to 26 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.
Sponsored by Universidad Miguel Hernandez de Elche · Not applicable, Interventional, and Prevention
This study evaluated the effects of a 12-week physiotherapy exercise programme on pelvic floor and abdominopelvic function in healthy young nulliparous women. Participants were randomly allocated to an intervention group or a control group. The intervention included supervised and home-based exercises focused on postural organization, breathing coordination, and lumbopelvic-abdominal muscle control. The control group continued their usual activities without receiving the study intervention. Pelvic floor muscle function, abdominopelvic functional responses, respiratory function, and health-related quality of life were assessed.
Universidad Miguel Hernandez de Elche is the lead sponsor of 84 studies on the registry; 15 are open to participants now.
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Exclusion Criteria:
Participants assigned to this group completed a 12-week physiotherapy exercise programme focused on postural organization, breathing coordination, and lumbopelvic-abdominal muscle control, combining supervised sessions with home-based exercise.
Behavioral: Multimodal Physiotherapy Exercise Programme
Participants assigned to this group continued their usual activities and did not receive the study exercise programme during the 12-week study period.
Participants completed a 12-week exercise programme combining postural organization, breathing coordination, and lumbopelvic-abdominal motor control. The programme included a 20-minute supervised session once weekly, complemented by home-based exercise.
Subumbilical Cough Test
Qualitative assessment of abdominal wall response during coughing. The outcome was categorized as no bulging or bulging of the abdominal wall. Bulging was defined as caudal bulging of the umbilicopubic region during the cough maneuver, indicating insufficient abdominal muscle activation.
Time frame: Baseline and after the 12-week intervention
Pelvic Floor Muscle Strength - Modified Oxford Scale
Pelvic floor muscle strength was assessed by digital vaginal palpation using the Modified Oxford Scale, scored from 0 to 5, where 0 indicates no perceptible muscle contraction and 5 indicates a strong contraction.
Time frame: Baseline and after the 12-week intervention
Pelvic Floor Muscle Endurance
Pelvic floor muscle endurance was assessed by vaginal perineometry. Participants performed three maximal pelvic floor muscle contractions, each maintained for as long as possible. Endurance was recorded as the duration of the sustained contraction, expressed in seconds.
Time frame: Baseline and after the 12-week intervention
Pelvic Floor Muscle Contraction Pressure
Pelvic floor muscle contraction pressure was assessed by vaginal perineometry using a pressure probe. Participants performed three maximal pelvic floor muscle contractions, and contraction pressure was recorded in cmH2O.
Time frame: Baseline and after the 12-week intervention
Abdominal Diastasis Functional Test
Abdominal wall function was assessed by palpation of the linea alba in the supraumbilical and infraumbilical regions, at rest and during trunk elevation. The test evaluated the presence or absence and location of abdominal diastasis and the response of the linea alba during abdominal muscle activation.
Time frame: Baseline and after the 12-week intervention
Transversus Abdominis Activation Test
Abdominal wall response was assessed during maximal inspiration and expiration. During maximal expiration, the outcome was categorized according to whether the abdomen protruded ("pushes") or did not protrude ("does not push"), reflecting the activation response of the transversus abdominis.
Time frame: Baseline and after the 12-week intervention
Forced Vital Capacity (FVC)
Forced vital capacity was assessed by forced spirometry using a DATOSPIR-120 spirometer. Three measurements were performed and the best measurement was recorded. FVC was expressed in liters.
Time frame: Baseline and after the 12-week intervention
Forced Expiratory Volume in One Second (FEV1)
Forced expiratory volume in one second was assessed by forced spirometry using a DATOSPIR-120 spirometer. Three measurements were performed and the best measurement was recorded. FEV1 was expressed in liters.
Time frame: Baseline and after the 12-week intervention
Peak Expiratory Flow (PEF)
Peak expiratory flow was assessed by forced spirometry using a DATOSPIR-120 spirometer. Three measurements were performed and the best measurement was recorded. PEF was expressed in liters per second (L/s).
Time frame: Baseline and after the 12-week intervention
Health-Related Quality of Life - SF-12
Health-related quality of life was assessed using the 12-item Short Form Health Survey (SF-12). Physical and mental health component scores were calculated, with higher scores indicating better perceived health-related quality of life.
Time frame: After the 12-week intervention
No study locations are listed for this record.
Plan to share: No — No prospective plan for individual participant data sharing was established for this study.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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Universidad Miguel Hernandez de Elche