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Postpartum Exercise Intervention

21 maj 2026 uppdaterad av: Rita Deering, Carroll University

Influence of a Supervised Postpartum Exercise Program on Maternal Physical Activity Levels and Musculoskeletal Health

The postpartum period is associated with decreases in physical activity levels, muscular strength, muscular endurance, and pelvic floor muscle function, but little scientific evidence exists on how best to initiate and progress exercise in the postpartum period. This proposal aims to improve habitual physical activity levels, neuromuscular health (i.e., strength, fatigability, symptom burden) and overall wellbeing (i.e., decreased fear of movement, improved sleep quality, improved perception of quality of life) through participation in a weekly exercise program. This study will help to inform postpartum exercise recommendations and is novel as it allows participants to incorporate their children into the exercise routine, thus removing a primary barrier to physical activity/exercise.

Studieöversikt

Status

Rekrytering

Betingelser

Intervention / Behandling

Detaljerad beskrivning

Physical activity (PA)/exercise is crucial for maternal health and wellbeing but several barriers to PA/exercise participation exist in the postpartum period. Musculoskeletal impairments-such as weakness, increased fatigability, pelvic floor dysfunction (e.g., incontinence, pelvic organ prolapse, etc.), and pain-are common in the postpartum period. While these impairments provide strong rationale for participation in PA/exercise, they can also act as barriers to participation. Several psychosocial barriers also exist, including fear of movement and lack of childcare. Despite the importance of PA/exercise for health and wellness, and the documented musculoskeletal impairments that are associated with the postpartum period, assessment of neuromuscular function and education on resuming exercise is lacking in the standard postpartum care model in the United States. In addition, conflicting information can be found on social media and among clinical experts on when and how to best resume PA/exercise after childbirth. This proposal will evaluate the influence of an eight-week exercise intervention on neuromuscular function (i.e., lower extremity strength & endurance, pelvic floor muscle strength & endurance, self-reported pelvic floor dysfunction symptoms), habitual physical activity levels, and overall wellbeing (i.e., levels of kinesiophobia, sleep quality, self-reported quality of life) in postpartum females. In an effort to decrease barriers to exercise, childcare will be offered, and participants will have the opportunity to incorporate their child(ren) into exercise sessions if they so desire. This proposal will utilize a randomized control trial (RCT) design and objective measures of strength (i.e., load cells) along with standard clinical assessments of pelvic floor muscle function (i.e., internal vaginal assessment of strength and endurance, self-reported symptoms using validated questionnaires).

Studietyp

Interventionell

Inskrivning (Beräknad)

50

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

  • Förenta staterna
    • Wisconsin
      • Waukesha, Wisconsin, Förenta staterna, 53186
        • Rekrytering
        • Carroll University Center for Graduate Studies
        • Kontakt:
        • Kontakt:
        • Huvudutredare:
          • Rita E Deering, DPT, PhD

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  • 18 years of age or older
  • gave birth in the 24 months prior to study enrollment

Exclusion Criteria:

  • less than 6 weeks postpartum or not medically appropriate to engage in exercise regardless of time since childbirth (will be screened using the Get Active Questionnaire for Postpartum)
  • prescription anti-inflammatory/pain medications that are taken daily;
  • significant orthopedic conditions that would contraindicate performance of the fatigue task and participation in the exercise intervention (such as fractures, severe scoliosis, etc)
  • moderate to severe cardiovascular &/or pulmonary disease that contraindicates participation in exercise
  • neuromuscular health conditions (such as diabetes, neuropathy, multiple sclerosis, stroke, seizures, etc);
  • smoking/vaping or use of other tobacco or nicotine products (chewing tobacco, nicotine patches, nicotine gum, etc.)
  • use of any illegal drugs

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Exercise Intervention
Study participants will attend a 1-hour in-person group exercise intervention once a week for 8 weeks.
Diagnostiskt test: Aktivt test för raka benhöjningar
ASLR-testet är ett väletablerat kliniskt test som bedömer stabiliteten i ländryggen/bäckenet, svårighetsgraden av bakre bäckensmärta och förmågan att aktivera magmusklerna. Det utförs i liggande. Deltagarna instrueras att höja ett ben, med knät rakt, till en hälhöjd av 20 cm. Benet hålls upptill i 5 sekunder och sänks sedan långsamt till marken. Deltagaren uppmanas att rapportera upplevd svårighet att höja benet på en skala från 0 till 5 (0=inte alls svårt; 5=kan inte lyfta benet) och smärta på en skala från 0 till 10 (0=ingen smärta; 10=värst möjlig smärta). Om svårighet eller smärta bedöms till 1 eller högre, upprepas testet med forskaren som ger extern kompression av bäckenet. Om upplevd svårighet eller rapporterad smärta är lägre med kompression, anses testet vara positivt för lumbopelvis instabilitet. Testet upprepas sedan på motsatt extremitet.
Andra namn:
  • ASLR-test
Övrig: Aktiv raka ben höjer trötthetsuppgift
Protokollet liknar ASLR-testet, förutom att deltagaren instrueras att hålla det upphöjda benet från marken så länge som möjligt. En luftmanschett med biofeedback kommer att placeras under deltagarens ländryggsregion för att bedöma rörelsen av ryggraden/bäckenet. Manschetten kommer att blåses upp till 40 mm Hg och deltagaren instrueras att hålla nålen så nära 40 mm Hg som möjligt under hela testet; ingen information kommer att ges om hur man påverkar manschetttrycket, men visuell återkoppling av manschetttrycket kommer att ges under hela uppgiften. Betyg av upplevd ansträngning (RPE) och smärta kommer att erhållas från deltagarna var 30-60:e sekund. Uppgiftsfel kommer att definieras som en hälhöjd ≤10 cm eller en förändring i manschetttrycket ≥20 mm Hg. Båda extremiteterna kommer att testas, men i olika pass. Ordningen för lemtestning (dominant vs icke-dominant) kommer att vara randomiserad och balanserad. Lemdominans kommer att rapporteras själv.
Diagnostiskt test: Ultraljudsundersökning av bukväggen
Ultraljud i realtid kommer att användas för att bedöma avstånd mellan räta punkter över och under naveln. Deltagarna kommer att bedömas med B-lägesbilder i ryggläge i vila, liggande medan de lyfter huvudet och i ryggläge när de utför en rak benhöjning. Principle Investigator har utbildning och erfarenhet av muskuloskeletalt ultraljud.
Övrig: Progressive exercise
A progressive, 8-week exercise intervention has been developed and will be administered in a group setting.
Andra namn:
  • Träning
Övrig: Lower Extremity Strength Testing
A straight leg raise maximal voluntary contraction (MVC) of each lower extremity an MVC of the hip extensors of the grounded limb will be performed in supine before and within 2 minutes of completing the ASLR fatigue task. The straight leg raise MVC will be performed with a custom-made load cell instrumented strength testing device, which consists of a rigid platform on which the participant will lie. At the foot of the device is a tower that houses 2 load cells connected to a lightly padded push plate. The hip extension MVC will be performed on a force plate. Before the ASLR fatigue task, a minimum of 3 MVC trials will be performed for each muscle group, with a minimum of 1 minute rest between trials; the highest peak force will be considered the MVC. Only 1 MVC trial per muscle group will be performed following the ASLR Fatigue Task.
Övrig: Pelvic Floor Muscle Strength Testing
An internal vaginal pelvic floor muscle assessment will be performed at baseline and study completion by a licensed physical therapist with advanced training in pelvic floor muscle examination and treatment. Pelvic floor muscle function will be assessed using the PERFECT scale, which assesses both muscular strength ("P" for "power") and endurance ("E"). Strength is assessed by cueing the participant to perform a maximal voluntary pelvic floor muscle contraction while the examiner has their index finger inserted into the vagina. The modified Oxford scale is used to grade strength on a scale of zero (0) to five (5).
Övrig: Pelvic Floor Muscle Endurance Testing
Pelvic floor muscle endurance is also assessed via the internal vaginal PFM examination. After strength testing is performed, participants are instructed to perform a maximal PFM contraction and hold for as long as possible (maximum of 10 seconds). The examiner counts the length of the contraction, and timing is stopped either when (1) strength of the contraction declines or (2) the maximum of 10 seconds is reached. The time in seconds is recorded.
Aktiv komparator: Control
Study participants will not receive the exercise intervention but will complete a weekly questionnaire to self-report physical activity levels.
Diagnostiskt test: Aktivt test för raka benhöjningar
ASLR-testet är ett väletablerat kliniskt test som bedömer stabiliteten i ländryggen/bäckenet, svårighetsgraden av bakre bäckensmärta och förmågan att aktivera magmusklerna. Det utförs i liggande. Deltagarna instrueras att höja ett ben, med knät rakt, till en hälhöjd av 20 cm. Benet hålls upptill i 5 sekunder och sänks sedan långsamt till marken. Deltagaren uppmanas att rapportera upplevd svårighet att höja benet på en skala från 0 till 5 (0=inte alls svårt; 5=kan inte lyfta benet) och smärta på en skala från 0 till 10 (0=ingen smärta; 10=värst möjlig smärta). Om svårighet eller smärta bedöms till 1 eller högre, upprepas testet med forskaren som ger extern kompression av bäckenet. Om upplevd svårighet eller rapporterad smärta är lägre med kompression, anses testet vara positivt för lumbopelvis instabilitet. Testet upprepas sedan på motsatt extremitet.
Andra namn:
  • ASLR-test
Övrig: Aktiv raka ben höjer trötthetsuppgift
Protokollet liknar ASLR-testet, förutom att deltagaren instrueras att hålla det upphöjda benet från marken så länge som möjligt. En luftmanschett med biofeedback kommer att placeras under deltagarens ländryggsregion för att bedöma rörelsen av ryggraden/bäckenet. Manschetten kommer att blåses upp till 40 mm Hg och deltagaren instrueras att hålla nålen så nära 40 mm Hg som möjligt under hela testet; ingen information kommer att ges om hur man påverkar manschetttrycket, men visuell återkoppling av manschetttrycket kommer att ges under hela uppgiften. Betyg av upplevd ansträngning (RPE) och smärta kommer att erhållas från deltagarna var 30-60:e sekund. Uppgiftsfel kommer att definieras som en hälhöjd ≤10 cm eller en förändring i manschetttrycket ≥20 mm Hg. Båda extremiteterna kommer att testas, men i olika pass. Ordningen för lemtestning (dominant vs icke-dominant) kommer att vara randomiserad och balanserad. Lemdominans kommer att rapporteras själv.
Diagnostiskt test: Ultraljudsundersökning av bukväggen
Ultraljud i realtid kommer att användas för att bedöma avstånd mellan räta punkter över och under naveln. Deltagarna kommer att bedömas med B-lägesbilder i ryggläge i vila, liggande medan de lyfter huvudet och i ryggläge när de utför en rak benhöjning. Principle Investigator har utbildning och erfarenhet av muskuloskeletalt ultraljud.
Övrig: Lower Extremity Strength Testing
A straight leg raise maximal voluntary contraction (MVC) of each lower extremity an MVC of the hip extensors of the grounded limb will be performed in supine before and within 2 minutes of completing the ASLR fatigue task. The straight leg raise MVC will be performed with a custom-made load cell instrumented strength testing device, which consists of a rigid platform on which the participant will lie. At the foot of the device is a tower that houses 2 load cells connected to a lightly padded push plate. The hip extension MVC will be performed on a force plate. Before the ASLR fatigue task, a minimum of 3 MVC trials will be performed for each muscle group, with a minimum of 1 minute rest between trials; the highest peak force will be considered the MVC. Only 1 MVC trial per muscle group will be performed following the ASLR Fatigue Task.
Övrig: Pelvic Floor Muscle Strength Testing
An internal vaginal pelvic floor muscle assessment will be performed at baseline and study completion by a licensed physical therapist with advanced training in pelvic floor muscle examination and treatment. Pelvic floor muscle function will be assessed using the PERFECT scale, which assesses both muscular strength ("P" for "power") and endurance ("E"). Strength is assessed by cueing the participant to perform a maximal voluntary pelvic floor muscle contraction while the examiner has their index finger inserted into the vagina. The modified Oxford scale is used to grade strength on a scale of zero (0) to five (5).
Övrig: Pelvic Floor Muscle Endurance Testing
Pelvic floor muscle endurance is also assessed via the internal vaginal PFM examination. After strength testing is performed, participants are instructed to perform a maximal PFM contraction and hold for as long as possible (maximum of 10 seconds). The examiner counts the length of the contraction, and timing is stopped either when (1) strength of the contraction declines or (2) the maximum of 10 seconds is reached. The time in seconds is recorded.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Average Total Activity Counts (TAC) per day over 7 days
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring the TAC per day. TAC is the total number of filtered, full-wave rectified, integrated accelerations (all directions). These will then be averaged/day based on the total number of valid wear days for each participant.
7 days pre-intervention, 7 days post-intervention
Physical Activity Measured by Average Steps per day over 7 days
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring mean steps per day. This will be quantified as reported by the Ametris (formerly ActiGraph) accelerometer and CentrePoint analysis software. The Algorithm used by Ametris is not publicly available, but Ametris/ActiGraph accelerometers are frequently used in research quantifying physical activity.
7 days pre-intervention, 7 days post-intervention
Mean Duration per day of Moderate-Vigorous Physical Activity (MVPA) over 7 days: tri-axial counts
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring mean duration per day of MVPA. Intensity of physical activity assessed using tri-axial counts (per the accelerometer software) are as follows: Light physical activity is between 200 and 2690 counts/min, moderate intensity between 2690-6166 counts/min, and vigorous intensity is ≥ 6167 counts/min. MVPA is ≥2690.
7 days pre-intervention, 7 days post-intervention
Mean Duration per day of Moderate-Vigorous Physical Activity (MVPA) over 7 days: vertical counts
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring mean duration per day of MVPA. Intensity of physical activity assessed using vertical counts (per the accelerometer software) are as follows: Light physical activity is between 100 and 759 counts/min, moderate intensity is 760-5999 counts/min, and vigorous intensity is ≥ 6000 counts/min (MVPA is > 760 counts/min).
7 days pre-intervention, 7 days post-intervention
Average Minutes per Day of Activity in at least 5-minute bouts
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring mean duration per day of all activity. Average minutes per day of activity within each of the following categories: light = 25.8 mg - 100.5 mg; moderate = 100.6 mg - 428.7 mg; vigorous = > 428.8 mg (mg is the vector magnitude of acceleration calculated in gravities using Euclidean Norm minus 1 metric)
7 days pre-intervention, 7 days post-intervention
Average Minutes per Day of Activity in at least 10-minute bouts
Tidsram: 7 days pre-intervention, 7 days post-intervention
Physical activity habits around the time of testing will be assessed with a tri-axial accelerometer for 7 days outside of the laboratory, in part by measuring mean duration per day of all activity. Average minutes per day of activity within each of the following categories: light = 25.8 mg - 100.5 mg; moderate = 100.6 mg - 428.7 mg; vigorous = > 428.8 mg. (mg is the vector magnitude of acceleration calculated in gravities using Euclidean Norm minus 1 metric)
7 days pre-intervention, 7 days post-intervention
Physical activity levels via self-reported questionnaires
Tidsram: Once-a-week for the 8-week intervention period
Participants will complete the International Physical Activity Questionnaire (IPAQ) short-form. The IPAQ short-form quantifies physical activity (PA) over the previous week in 2 categories: low, moderate, or high activity; or metabolic equivalents (MET) minutes per week. High PA is categorized as (1)vigorous PA on at least 3 days/week with a combined minimum of at least 1500 MET minutes/week or (2) 7 days of cumulative PA of any intensity that sums to a minimum total of at least 3000 MET minutes/week. Moderate PA is categorized as (1) 3+ days of at least 30 minutes of vigorous PA, (2) 5+ days of moderate PA or walking at least 30 minutes/day, or (3) 5+ days of any level of PA that sums to a minimum of 600 MET minutes/week. Low physical activity is categorized as activity that does not meet the criteria for medium or high activity.
Once-a-week for the 8-week intervention period
Lower extremity strength
Tidsram: Baseline and 7-14 days post-intervention
A straight leg raise maximal voluntary contraction (MVC) of each lower extremity will be performed in supine before and within 2 minutes of completing the ASLR fatigue task with a custom made load cell instrumented strength testing device. This device consists of a rigid platform on which the study participant will lie supine. At the foot of the device is a tower that houses 2 load cells and is connected to a lightly padded push plate. This push plate can be raised and lowered such that the participant can push up into the plate (contacts the anterior surface of the participant's shin) or push down onto the push plate (contacts the posterior aspect of the participant's heel). Before the ASLR fatigue task, a minimum of 3 MVC trials will be performed on each leg, with a minimum of 1 minute rest between trials; the highest peak force will be considered the MVC. Only 1 MVC trial per leg will be performed following the fatigue task.
Baseline and 7-14 days post-intervention
Mean Time to ASLR Fatigue Task Failure
Tidsram: Baseline and 7-14 days post-intervention
The Active Straight Leg Raise Fatigue Task will be administered. Participants are asked to raise one leg to a heel height of 20 cm while lying supine. Participants are encouraged to keep the leg raised as long as possible. Task failure will be defined as a heel height less than or equal to 10 centimeters off the ground.
Baseline and 7-14 days post-intervention
Pelvic floor muscle strength
Tidsram: Baseline and 7-14 days post-intervention
An internal vaginal pelvic floor muscle assessment will be performed at baseline and study completion by a licensed physical therapist with advanced training in pelvic floor muscle examination and treatment. Pelvic floor muscle function will be assessed using the PERFECT scale, which assesses both muscular strength ("P" for "power") and endurance ("E"). Strength is assessed by cueing the participant to perform a maximal voluntary pelvic floor muscle contraction while the examiner has their index finger inserted into the vagina. The modified Oxford scale is used to grade strength on a scale of zero (0) to five (5) with 5 being the strongest.
Baseline and 7-14 days post-intervention
Pelvic floor muscle endurance
Tidsram: Baseline and 7-14 days post-intervention
Pelvic floor muscle endurance is also assessed via the internal vaginal PFM examination. After strength testing is performed, participants are instructed to perform a maximal PFM contraction and hold for as long as possible (maximum of 10 seconds). The examiner counts the length of the contraction, and timing is stopped either when (1) strength of the contraction declines or (2) the maximum of 10 seconds is reached.55 The time in seconds is recorded.
Baseline and 7-14 days post-intervention
Mean Pelvic Floor Distress Inventory Short Form (PFDI-20) Score
Tidsram: Baseline and 7-14 days post-intervention
The PFDI-20 is composed of 20 items total on three scales (Pelvic Organ Prolapse, Colorectal-Anal Distress, Urinary Distress), each scored on a 5 point likert scale. Mean scores from each scale are calculated and multiplied by 25, then added together for a total possible range of scores from 0-300. Higher scores indicate increased pelvic floor distress.
Baseline and 7-14 days post-intervention
Fear of movement
Tidsram: Baseline and 7-14 days post-intervention
Fear of movement (kinesiophobia) will be assessed via the Tampa Scale for Kinesiophobia (TSK). The TSK is a 17-question, self-administered questionnaire that utilizes a 4-point Likert scale (1= strongly agree, 4=strongly disagree). Total scores range from 17-68. A higher score indicates higher levels of kinesiophobia; a score of 17 indicates no/minimal kinesiophobia.
Baseline and 7-14 days post-intervention
Overall quality of life
Tidsram: Baseline and 7-14 days post-intervention
Participants will complete the SF-20 questionnaire, which measures health in six different domains (physical functioning, role functioning, social functioning, mental health, health perceptions, and pain). Scores range from 0-100%, with 0% being the worst score and 100% being the best.
Baseline and 7-14 days post-intervention
Mean Global Pittsburgh Sleep Quality Index (PSQI) Score
Tidsram: Baseline and 7-14 days post-intervention
The PSQI assesses seven sleep domains: sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medications, and daytime dysfunction. The seven components scores are then added to yield a global PSQI score in the range of zero to 21. Higher scores indicate worse sleep quality. A global score greater than five is diagnostic of poor sleep quality.
Baseline and 7-14 days post-intervention
Inter-recti distance
Tidsram: Baseline and 7-14 days post-intervention
Ultrasound imaging will be used to measure the distance between the right and left rectus abdominis at 2 locations above the umbilicus and 2 locations below the umbilicus. IRD will be assessed in supine at rest (end exhalation), while lifting the head, and while lifting one leg.
Baseline and 7-14 days post-intervention

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Assessment of fatigability of the lumbopelvic stabilizing muscles measured by the ASLR Fatigue Task: Mean Pain Score
Tidsram: Baseline and 7-14 days post-intervention
For the ASLR Fatigue Task, the participant is instructed to maintain the elevated leg off the ground for as long as possible. A biofeedback air cuff placed under the participant's lumbopelvic region assesses movement of the spine/pelvis during the test. The cuff will be inflated to 40 mm Hg, and the participant will be instructed to keep the needle as close to 40 mm Hg as possible throughout the test. Pain Scores will be measured (0-10 with higher scores increased pan) every 30-60 seconds. Task failure will be defined as a heel height ≤10 cm or a change in cuff pressure ≥20 mm Hg.
Baseline and 7-14 days post-intervention
Percent Change in Global Surface EMG Recordings: Abdominal Muscles
Tidsram: Baseline and 7-14 days post-intervention
Electromyography (EMG) will be reported as the root mean square (RMS) value. The percent change in EMG from the start of the ASLR Fatigue task to task failure will be examined.
Baseline and 7-14 days post-intervention
Percent Change in Global Surface EMG Recordings: Rectus femoris
Tidsram: Baseline and 7-14 days post-intervention
EMG for the rectus femoris will be normalized to the maximum RMS EMG obtained during lower extremity strength testing. The percent change in EMG from the start of the task to task failure will be examined.
Baseline and 7-14 days post-intervention

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Root mean square (RMS) of global EMG
Tidsram: Baseline and 7-14 days post-intervention
Muscle behavior will be quantified from surface EMG recordings of the rectus abdominis and rectus femoris using multi-channel array surface EMG electrodes during maximal and submaximal contractions and fatiguing exercise of the abdominal muscles. If successful, RMS of global EMG will be reported.
Baseline and 7-14 days post-intervention
Percent of Maximum Voluntary Isometric Contraction (MVIC)
Tidsram: Baseline and 7-14 days post-intervention
Muscle activity will be quantified from surface EMG recordings of the rectus abdominis and rectus femoris using a multi-channel array surface EMG electrodes during submaximal contractions and fatiguing exercise of the abdominal muscles, and normalized to the RMS EMG during maximal voluntary isometric contractions (MVIC). If successful, percent of MVIC will be reported.
Baseline and 7-14 days post-intervention

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Carroll University

Utredare

  • Huvudutredare: Rita Deering, DPT, PhD, Carroll University
  • Studierektor: Kimberly Klug, DSc, Carroll University

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

19 februari 2026

Primärt slutförande (Beräknad)

1 maj 2028

Avslutad studie (Beräknad)

1 augusti 2028

Studieregistreringsdatum

Först inskickad

20 november 2025

Först inskickad som uppfyllde QC-kriterierna

21 maj 2026

Första postat (Faktisk)

29 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

29 maj 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

21 maj 2026

Senast verifierad

1 april 2026

Mer information

Termer relaterade till denna studie

Nyckelord

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • 2025-061

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

JA

IPD-planbeskrivning

Data will be archived in the NICHD Data and Specimen Hub (DASH). Per the DASH protocol, study data will be assigned a digital object identifier (DOI). Data will also be able to be found via searching for keywords (e.g., postpartum exercise).

Tidsram för IPD-delning

Data will be made available following completion of data collection. Data will be shared for as long as possible per DASH guidelines.

Kriterier för IPD Sharing Access

Data will be accessible to any person with access to DASH. Access to scientific data will not be controlled by study personnel. All 18 identifiers listed in the HIPAA Privacy Rule will be removed from data shared in the DASH repository to protect study participants.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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