RECRUITING

Orthopaedic Manual Physical Therapy as Part of the Postpartum Care Continuum

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Data shows us that injury risk increases in the first year postpartum. There is a paucity of literature regarding MSK injuries in postpartum military women. A unique challenge that postpartum service members face is the increased stress of training for and having to pass a physical fitness test directly tied to their career advancement. While there is epidemiological data across multiple branches of service, there is a gap in the literature in terms of how to appropriately address these decreased fitness levels and better understand the root causes. American College of Gynecology (ACOG) recommends that the postpartum visit include actionable information on return to physical activity. However, a large majority of women report receiving no guidance on how to engage in physical activity during pregnancy and in the postpartum period. Physical therapy is commonly used to help individuals return to physical activity following orthopaedic surgeries, but it is not frequently utilized to assist the postpartum population in progressing back to physical activity. Orthopaedic Manual Physical Therapists (OMPTs) are uniquely trained to address musculoskeletal symptoms and progress physical activity. An OMPT evaluation and treatment could facilitate increased physical activity and improve health-related quality of life, supporting the ACOG recommendation to make postpartum care an ongoing multidisciplinary process.

Official Title

Orthopaedic Manual Physical Therapy as Part of the Postpartum Care Continuum for Active-Duty Service Members

Quick Facts

Study Start:2024-04-08
Study Completion:2025-07-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06560190

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 44 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Female Active-Duty Service Member
  2. * Postpartum \>6 weeks and \<6 months
  3. * Cleared by OBGYN at postpartum follow-up to initiate physical activity
  1. * Current or ongoing treatment by an orthopaedic physical therapist
  2. * Separating from military service in the next 6 months
  3. * Current permanent profile for a musculoskeletal condition
  4. * Peripartum Hysterectomy

Contacts and Locations

Study Contact

Casey Shutt-Hoblet, DPT
CONTACT
210-808-2226
casey.e.shutt-hoblet.mil@health.mil

Principal Investigator

Casey Shutt-Hoblet, DPT
PRINCIPAL_INVESTIGATOR
Brooke Army Medical Center

Study Locations (Sites)

Brooke Army Medical Center
San Antonio, Texas, 78234
United States

Collaborators and Investigators

Sponsor: Brooke Army Medical Center

  • Casey Shutt-Hoblet, DPT, PRINCIPAL_INVESTIGATOR, Brooke Army Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-08
Study Completion Date2025-07-05

Study Record Updates

Study Start Date2024-04-08
Study Completion Date2025-07-05

Terms related to this study

Keywords Provided by Researchers

  • Postpartum
  • Physical Activity
  • Pregnancy
  • Service Member
  • Physical Therapy

Additional Relevant MeSH Terms

  • Postpartum
  • Pregnancy Related