Clinical Trials Logo

Clinical Trial Summary

The purpose of this research is to investigate the effectiveness of a personalised physical training programme in returning servicewomen to fitness following childbirth. The idea behind the program is to target core and pelvic floor muscles, along with whole body strength and endurance to help servicewomen return to work safely and in a physically fit condition. The study will monitor the response to training using the following measures: urogynaecological measures (e.g., pelvic floor strength, prolapse, urinary incontinence), military specific fitness tests, musculoskeletal health (e.g., muscle and bone mass & function) and mental health and wellbeing.


Clinical Trial Description

In an independent groups study design, the aim was to investigate the efficacy of a postpartum physical development programme on core reconnection (i.e., pelvic floor function, core strength/stability and urogynaecological measures), occupational physical performance, musculoskeletal health, and psychological health/wellbeing in servicewomen. Given that policy guidance is urgently needed regarding the safe return of servicewomen to functional occupational fitness, the aim of our proposed research is to inform the appropriate physical preparation of servicewomen in the postpartum period. Participants at selected sites around the Royal Military Academy at Sandhurst will receive usual care/no formal intervention (acting as a control group [CON]) and participants at different sites around Army Headquarters will receive usual care and additionally complete an 18-week phased physical development (rehabilitation and training) programme between weeks 6 and 24 postpartum (acting as the intervention group [INT]). If recruitment numbers are low at the main sites (Aldershot and Tidworth) we will seek to recruit participants to INT from Bulford, Middle Wallop, Larkhill and Marlborough Lines for INT and to CON from Sandhurst, Odiham, Pirbright, Keogh, Minley, Deepcut as well as locations outside of the named INT sites. The geographical separation of sites was deemed to be important for maintaining differences between intervention and control group activity. The investigators have designed a phased 18-week physical development programme to train both rehabilitative and performance enhancement elements of physical preparation. The rehabilitation element of the programme will specifically target pelvic floor function and core strength and stability (known collectively as Core Reconnection training) from weeks 6 to 24 postpartum, and the training element of the programme will contain resistance and high-intensity interval training (HIIT) from weeks 12 to 24 postpartum The aim of this research is to investigate the effectiveness of a tailored rehabilitation and physical preparation programme for postpartum women on: 1. Occupational fitness performance; 2. Female health assessments (i.e., urinary incontinence, pelvic floor strength); 3. Musculoskeletal health; 4. Psychological health and wellbeing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04332757
Study type Interventional
Source Nottingham Trent University
Contact Craig Sale, PhD
Phone +44(0)115 848 3505
Email craig.sale@ntu.ac.uk
Status Recruiting
Phase N/A
Start date July 4, 2019
Completion date September 20, 2022

See also
  Status Clinical Trial Phase
Completed NCT00001867 - Effect of Pregnancy on Uveitis N/A
Active, not recruiting NCT03703804 - AfterBabyBodyStudy- Testing Manual Examination Methods and Exercise Effects on Muscular Recovery After Pregnancy
Completed NCT04153760 - Pilot PARTUM Trial: Postpartum Aspirin to Reduce Thromboembolism Undue Morbidity Early Phase 1
Completed NCT03004872 - Relationship Between Postpartum Mood Disorders and Delivery Experience
Completed NCT01272960 - Mirena Intrauterine System Timing of Insertion: A Randomized Controlled Trial N/A
Completed NCT00563264 - KAN-DO: A Family-based Intervention to Prevent Childhood Obesity N/A
Active, not recruiting NCT05510284 - Post-partum Care in the NICU N/A
Completed NCT04238117 - Laser Acupuncture Therapy in Postpartum Low Back Pain N/A
Completed NCT04977713 - Delivery Pain and Postpartum Comfort N/A
Completed NCT04389489 - Postpartum Sexual Function in Pregnant Women With COVID-19
Completed NCT04783324 - The Effect of the E-Mobile Health Application on Postpartum Adaptation N/A
Completed NCT01020240 - Physiotherapy in Postpartum After a Cesarean N/A
Completed NCT03436888 - Cross-cultural Adaptation and Validation of the Pelvic Girdle Questionnaire in French Language
Active, not recruiting NCT05674461 - The Effect of WhatsApp-Based and Face-to-face Nursing Education on Mothers' Quality of Life and Traditional Practices N/A
Recruiting NCT05188963 - RCT About Two Different Regimens of Clean Intermittent Catheterization in Women With Overt Postpartum Urinary Retention N/A
Completed NCT00998595 - Gestational Diabetes Follow Up Study N/A
Enrolling by invitation NCT06119282 - The Effect of Aromatherapy in Women With Primiparous Cesarean Section N/A
Completed NCT02781714 - Evaluation of an mHealth SMS Dialogue Strategy to Meet Women's and Couples' Postpartum Contraceptive Needs in Kenya N/A
Completed NCT00828542 - Safety of the Etonogestrel-Releasing Implant During the Puerperium of Healthy Women N/A
Completed NCT05439668 - Comparison of Two Abdominal Exercise Programs on the Interrect Distance N/A