Hamstring Strengthening in Hypermobile Conditions
perjantai 29. toukokuuta 2026 päivittänyt: Ranita Manocha, University of Calgary
Effects and Feasibility of Eccentric Hamstring Strengthening in Hypermobility Spectrum Disorders and Hypermobile Ehlers-Danlos Syndrome
The goal of this clinical trial is to determine how strengthening the hamstring muscles affects the knee joint in people living with hypermobility spectrum disorders (HSD) and hypermobile Ehlers-Danlos syndrome (hEDS). The main questions it aims to answer are:
- Does hamstring strengthening reduce the looseness of the knee joint in HSD/hEDS?
- Does hamstring strengthening improve clinical outcomes like pain in people living with HSD/hEDS?
Participants will:
- Attend two exercise classes per week for 12 weeks.
- Visit the laboratory every 4-6 weeks for testing.
Tutkimuksen yleiskatsaus
Tila
Ei vielä rekrytointia
Ehdot
Yksityiskohtainen kuvaus
Hypermobility spectrum disorders (HSD) and hypermobile Ehlers-Danlos syndrome (hEDS) affect 1 in 500 people, predominantly females.
While exercise is known to be beneficial for HSD/hEDS, the effect of eccentric exercise on passive joint stability, the functional capacity to perform daily activities, and quality of life remains unknown.
This clinical trial aims to determine the effects of a 12-week eccentric hamstring strengthening intervention for females with HSD/hEDS on knee joint laxity, performance during walking and stair climbing, and quality of life.
This study will have important implications for understanding the impacts of exercise in HSD/hEDS.
This can then inform clinical guidance and recommendations around lower limb exercise for this population.
Opintotyyppi
Interventio
Ilmoittautuminen (Arvioitu)
20
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.
Opiskeluyhteys
- Nimi: Ranita Manocha
- Puhelinnumero: 4039444224
- Sähköposti: bettermobilitylab@ucalgary.ca
Opiskelupaikat
-
-
Alberta
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Calgary, Alberta, Kanada, T2N 4N1
- University of Calgary - Foothills Campus
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Ottaa yhteyttä:
- Ranita Manocha
- Sähköposti: bettermobilitylab@ucalgary.ca
-
Päätutkija:
- Ranita Manocha, MD, MSc
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Osallistumiskriteerit
Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
Hyväksyy terveitä vapaaehtoisia
Ei
Kuvaus
Inclusion Criteria:
- Reported diagnosis of HSD or hEDS by a physician
- Meet the 2017 International Diagnostic Criteria for HSD and hEDS
- Clearance to participant in exercise participation, determined using the Get Active Questionnaire
Exclusion Criteria:
- Other acquired or hereditary connective tissue disorder (i.e., rheumatoid arthritis, Marfan syndrome, etc.)
- Currently experiencing daily knee pain
- Prior knee injury or surgery
- Intra-articular knee injection in the last 12 months
- Currently pregnant
Opintosuunnitelma
Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Perustiede
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: Eccentric hamstring exercise
All participants will complete a 12-week supervised lower limb strengthening program focused on eccentric hamstring loading.
Participants will complete two training sessions per week with at least 48 hours between training sessions.
Multiple classes will be offered each week to increase participation opportunity, with morning classes (8-9am) and evening classes (6-7pm) being offered on Mondays and Thursdays.
Each class will be led by the same trained kinesiologist and cover the same training protocol within a given week, regardless of the day or time.
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The exercise intervention consists of a 12-week supervised lower limb strengthening program focused on eccentric hamstring loading.
This program is adapted from a lower limb progressive resistance training protocol that was well-tolerated and effective in people with HSD/hEDS.
Each exercise session will start with a 10-minute aerobic warm up.
This will be followed by the lower limb strengthening exercises, and a 5-minute aerobic cooldown.
The lower limb exercises will include forward lunges and seated machine weights (leg press, leg extension, leg curl, calf raise).
At weeks 6-11, eccentric hamstring loading will be initiated by utilizing the 2:1 technique of two limbs performing concentric action at once and then a single limb performing the eccentric action in a seated leg curl machine.
This is an established eccentric loading protocol for the hamstring muscle group.
Muut nimet:
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Knee Joint Laxity
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Anterior knee joint laxity measured in millimeters using a KT-2000 Knee Ligament Arthrometer at 67N, 89N, and 133N of applied force, as well as maximum displacement.
Posterior knee joint laxity will be assessed at 67N of applied force.
Changes in knee joint laxity at each level of applied force will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Knee Joint Stiffness
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Anterior knee joint stiffness calculated from the change in displacement divided by the change in force from 0N to 67N, 67N to 89N, and 89N to 133N.
Posterior knee joint stiffness will be calculated between 0N and 67N of force.
Changes in stiffness will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isokinetic eccentric knee flexion strength
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isokinetic eccentric knee flexion strength at 60 degrees per second will be measured using a Biodex Dynamometer.
Change in eccentric knee flexion strength will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isokinetic concentric knee flexion strength
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isokinetic concentric knee flexion strength at 60 degrees per second will be measured using a Biodex dynamometer.
Change in concentric knee flexion strength will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Hamstrings:Quadriceps Co-Activation
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Co-activation between the hamstrings and quadriceps muscles will be measured using Delsys surface electromyography sensors during dynamometry, the 6-Minute Walk Test, and the stair climb test.
Changes in hamstring:quadriceps co-activation will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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6-Minute Walk Test
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Functional capacity/performance will be assessed using the 6-Minute Walk Test, which measures the distance in meters that a participant can walk in 6 minutes.
Changes in performance will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Pain Severity Score
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Pain severity score (from 0 to 40) will be calculated from the pain severity components of the Brief Pain Inventory.
The Brief Pain Inventory is a questionnaire that measures the location of pain (body diagram), pain severity (4 questions with numeric rating scales from 0-10, 0 indicating "no pain" and 10 indicating "pain as bad as you can imagine"), medications or treatments, a numeric rating scale (0-100%, 0% indicating "no relief" and 100% indicating "complete relief") for relief of pain from medications or treatments, as well as pain interference (7 questions with numeric rating scales from 0-10, 0 indicating "does not interfere" and 10 indicating "completely interferes").
Changes in pain severity score will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Safety of the Intervention
Aikaikkuna: Monitored throughout the study from baseline to 24 weeks.
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Safety of the intervention will be monitored and determined by the number of adverse events reported by participants to either the exercise kinesiologist during the exercise sessions, or to the research team during data collection or via email.
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Monitored throughout the study from baseline to 24 weeks.
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Tolerability of the Intervention
Aikaikkuna: Monitored throughout the study, from baseline to week 24.
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Tolerability of the exercise intervention will be assessed using the following metrics: Number of participants that withdraw from the study (along with reasons for withdrawal), number of exercises classes completed after 12 weeks, and pain severity (100mm visual analog scale) before and after each exercise class.
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Monitored throughout the study, from baseline to week 24.
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Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Acceptability of the Intervention
Aikaikkuna: Measured at the follow up visits for week 12, 18, and 24.
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Participants will be asked open ended questions via an online survey at 12, 18 and 24 weeks after baseline asking about how acceptable they found the exercise program to be.
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Measured at the follow up visits for week 12, 18, and 24.
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Adherence and Maintenance of Exercises
Aikaikkuna: Measured at follow up visits for week 12, 18, and 24.
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Adherence to the exercise program and maintenance of the exercises following completion of the 12 weeks of supervised classes will be assessed using open ended questions via an online survey send to participants at 12, 18, and 24 weeks after baseline.
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Measured at follow up visits for week 12, 18, and 24.
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Knee Joint Range of Motion
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Knee joint range of motion will be measured in degrees both actively and passively using a goniometer.
Changes in range of motion will be assessed from baseline, 4, 8 , 12, 18, and 24 weeks.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isometric knee flexion and extension strength
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Isometric knee flexion and extension strength will be measured using dynamometry at 90 degrees of knee flexion.
Changes in isometric flexion and extension strength will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Stair Climb Test
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Functional capacity/performance will also be assessed using a Stair Climb Test, which measures the time that a participant can ascend and descent a set of stairs.
Changes in performance will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Pain Interference Score
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Pain interference score (from 0 to 70) will be calculated from the pain severity components of the Brief Pain Inventory.
The Brief Pain Inventory is a questionnaire that measures the location of pain (body diagram), pain severity (4 questions with numeric rating scales from 0-10, 0 indicating "no pain" and 10 indicating "pain as bad as you can imagine"), medications or treatments, a numeric rating scale (0-100%, 0% indicating "no relief" and 100% indicating "complete relief") for relief of pain from medications or treatments, as well as pain interference (7 questions with numeric rating scales from 0-10, 0 indicating "does not interfere" and 10 indicating "completely interferes").Changes in pain interference score will be assessed from baseline to 4, 8, 12, 18, and 24 weeks after baseline.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Knee Pain
Aikaikkuna: Measured before and after each exercise class, and at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Knee pain will be determined before and after each exercise session using a 100mm visual analog scale (VAS), with 0 indicating "no pain" and 100 indicating "pain as bad as you can imagine".
Knee pain will also be determined at baseline and each follow up assessment using a 100mm VAS for the average knee pain over the last 7 days during rest and during walking, with 0 indicating "no pain" and 100 indicating "pain as bad as you can imagine".
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Measured before and after each exercise class, and at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Kinesiophobia
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Fear related to physical activity will be measured using the Tampa Scale for Kinesiophobia at baseline and each follow up assessment.
The Tampa Scale is scored from 17 questions related to pain, injury, physical activity, and fear.
The answers for each question are structured as a 4 point Likert scale (1 - "strongly disagree", 2 - "disagree", 3 - "agree", or 4 - "strongly agree").
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Fatigue
Aikaikkuna: Measured before and after each exercise class, and at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Generalized fatigue will be measured using the Fatigue Severity Scale (FSS) at baseline and each follow up assessment.
The FSS contains 9 questions relating to fatigue on a 7 point Likert scale.
A 100mm visual analog scale will also accompany the FSS asking to "indicate on the line the point that best describes your fatigue during the past week", with 0 indicating "very alert" and 100 indicating "extremely fatigued".
Additionally, a 100mm visual analog scale for fatigue will be measured before and after each exercise class with with 0 indicating "very alert" and 100 indicating "extremely fatigued".
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Measured before and after each exercise class, and at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Physical Activity Level
Aikaikkuna: Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Physical activity levels over the past 7 days will be quantified at baseline and at each follow up assessment using the International Physical Activity Questionnaire (IPAQ).
The IPAQ looks at the duration of time spent doing moderate or vigorous activities across job-related physical activity, transportation physical activity, housework/house maintenance/caring for family and recreation/sport/leisure time physical activity.
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Measured at all 6 outcome assessments (baseline, 4, 8, 12, 18, and 24 weeks).
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Impact of Hypermobility
Aikaikkuna: Measured at baseline and each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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The impacts of hypermobility on quality of life and physical function will be assessed using the Bristol Impact of Hypermobility (BiOH) questionnaire.
The BiOH is scored from 0 to 360, with higher scores indicating greater severity.
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Measured at baseline and each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Quality of Life
Aikaikkuna: Measured at baseline and each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Quality of life will also be measured using the RAND 36-item short form (SF-36).
The SF-36 contains 36 multiple choice questions that are reported as 8 domains, including physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, and general health.
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Measured at baseline and each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Knee Injury and Osteoarthritis Outcome Score
Aikaikkuna: Measured at baseline and at each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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The Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire which measures quality of life and functional outcomes within domains of pain, symptoms, activities of daily living, sport/recreation, and knee-related quality of life.
Each domain includes questions with 5-point Likert scales, including how often is your knee painful (never, monthly, weekly, daily, always), symptom severity (none, mild, moderate, severe, extreme), symptom presentations (never, rarely, sometimes, often, always), difficulty with activities (none, mild, moderate, severe, extreme), lifestyle modifications (not at all, mildly, moderately, severely, totally), and concerns (not at all, mildly, moderately, severely, extremely).
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Measured at baseline and at each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Knee Joint Proprioception
Aikaikkuna: Measured at baseline and at each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Knee joint proprioception will be measured with a joint angle reproduction test using isokinetic dynamometer.
The participant will be moved to a particular knee angle, then asked to reproduce this knee angle.
The error in degrees between the original joint angle and the participant's reproduced joint angle will be calculated.
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Measured at baseline and at each follow up assessment at 4, 8, 12, 18, and 24 weeks.
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Work Status
Aikaikkuna: Measured at baseline and each follow up assessment at 4, 8, 12, 18 and 24 weeks.
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Work Status will be reported at baseline and each follow up assessment as a multiple choice question with the following answers: not working by choice, part-time student, full-time student, retired, working full-time, working part-time, on temporary medical leave or short-term disability, on long-term disability (private, Canada Pension Plan Disability, or Workers' Compensation Board-Alberta income supplementation), other (please specify).
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Measured at baseline and each follow up assessment at 4, 8, 12, 18 and 24 weeks.
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Yhteistyökumppanit ja tutkijat
Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.
Sponsori
Tutkijat
- Päätutkija: Ranita Manocha, University Of Calgary
Opintojen ennätyspäivät
Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan julkisella verkkosivustolla.
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Maanantai 1. kesäkuuta 2026
Ensisijainen valmistuminen (Arvioitu)
Lauantai 1. toukokuuta 2027
Opintojen valmistuminen (Arvioitu)
Sunnuntai 1. elokuuta 2027
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Perjantai 29. toukokuuta 2026
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Perjantai 29. toukokuuta 2026
Ensimmäinen Lähetetty (Todellinen)
Torstai 4. kesäkuuta 2026
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Torstai 4. kesäkuuta 2026
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Perjantai 29. toukokuuta 2026
Viimeksi vahvistettu
Perjantai 1. toukokuuta 2026
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
- Tuki- ja liikuntaelinten sairaudet
- Verisuonisairaudet
- Sydän-ja verisuonitaudit
- Nivelsairaudet
- Geneettiset sairaudet, synnynnäiset
- Sidekudostaudit
- Hematologiset sairaudet
- Ihosairaudet
- Synnynnäiset poikkeavuudet
- Hemostaattiset häiriöt
- Hemorragiset häiriöt
- Ihosairaudet, geneettiset
- Ihon poikkeavuudet
- Kollageenisairaudet
- Synnynnäiset, perinnölliset ja vastasyntyneiden sairaudet ja poikkeavuudet
- Käyttäytyminen
- Iho- ja sidekudostaudit
- Hemic- ja imusuutteet
- Ehlers-Danlosin oireyhtymä
- Nivelten epävakaus
- Motorinen toiminta
- Ehlers-Danlos-oireyhtymä Tyyppi 3
- Moottoritoiminta
- Liike
- Tuki- ja liikuntaelinten fysiologiset ilmiöt
- Tuki- ja hermosto- ja hermostofysiologiset ilmiöt
- Käyttää
Muut tutkimustunnusnumerot
- REB26-0442
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
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Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .