Postpartum Exercise and Return to Fitness: Optimise Readiness for Military Mums (PERFORM)

NCT04332757 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2021-05-28

No results posted yet for this study

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.

Conditions

  • Postpartum Period

Interventions

OTHER

Training intervention.

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.

Sponsors & Collaborators

  • University of Nottingham

    collaborator OTHER
  • Robert Gordon University

    collaborator OTHER
  • University of Stirling

    collaborator OTHER
  • Ministry of Defence, United Kingdom

    collaborator OTHER_GOV
  • Clare Pacey Physiotherapy Limited

    collaborator UNKNOWN
  • Nottingham Trent University

    lead OTHER

Principal Investigators

  • Craig Sale, PhD · Nottingham Trent University

  • Kirsty Elliott-Sale, PhD · Nottingham Trent University

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-04
Primary Completion
2022-09-20
Completion
2022-09-20

Countries

  • United Kingdom

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 NCT04332757 on ClinicalTrials.gov