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The ADAPTation to Therapeutic Resistance Training (ADAPT) Study

Low-load Blood Flow Restriction Exercise Versus Conventional Heavier Load Resistance Training Exercise in UK Military Personnel With Persistent Knee Pain: A Multi-centre Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05719922
Enrollment
150
Registered
2023-02-09
Start date
2022-12-01
Completion date
2024-08-31
Last updated
2023-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Weakness, Musculoskeletal Injury

Keywords

Musculoskeletal rehabilitation, Blood flow restriction, Resistance training, knee pain, military

Brief summary

In 2018, the Academic Department of Military Rehabilitation (ADMR) published a pilot randomised controlled trial (RCT), demonstrating the feasibility and acceptability of integrating twice-daily blood flow restriction (BFR) training into a busy residential care setting. Following its publication was a guidance note written by the Directorate of Defence Rehabilitation restricting the implementation of BFR training until more evidence can be provided to support its efficacy. This research trial is a fully-powered, multi-centre RCT investigating the efficacy and biological mechanism underpinning BFR therapy in UK military personnel with lower-limb musculoskeletal injury (specifically, persistent anterior knee pain) during residential rehabilitation. This study will aim to optimise both the rehabilitation outcome and improve the time-and cost-effectiveness of the service delivered across UK Defence Rehabilitation and beyond. Results will provide insight and knowledge to the clinical and scientific community to not only those embedded within Defence Rehabilitation, but also those working in civilian sector organisations and professional sport in the UK and abroad.

Interventions

OTHERResistance Training

Comparing two different exercise-based treatment methodologies on the clinical outcomes of individuals with persistent knee pain.

Sponsors

University of Bath
CollaboratorOTHER
Defence Medical Rehabilitation Centre, UK
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* mechanical knee pain for at least three months * present with clinical signs and symptoms of knee pain arising from the tibiofemoral or patellofemoral joint diagnosed by sport and exercise medicine physician and/or physiotherapist * have reduced occupational employability medical grade secondary to their knee pain * report progression of resistance training load within the patient's rehabilitation programme is limited by knee pain * aged between 18 and 55 years * available to attend for the entire duration of the RRU course and a review appointment 3-months following course.

Exclusion criteria

diagnosed tibial, femoral or patella fracture and/or dislocation; * present with instability in the knee resulting from ligament deficiency * present with clinical signs and symptoms of patellar tendinopathy * have planned surgery over the study period * restricted knee range of movement; clinical signs and symptoms of non-musculoskeletal or serious pathological condition (i.e. Inflammatory arthropathy, infection or tumour) or referred pain from non-local pain source * present with any physical impairment or co-morbidities (including cardio-vascular disease) precluding the safe participation in the rehabilitation programme and/or assessment procedures * Cortico-steroid or analgesic injection intervention within the previous 7-days or previous knee surgery within the last 12 months to the affected limb Medical

Design outcomes

Primary

MeasureTime frameDescription
Change in Lower Extremity Functional Scale (LEFS) over timeBaseline, week 3 and week 15LEFS is a 20-question patient-reported outcome measure (PROM) that measures functional status in patients with lower limb musculoskeletal injury. Questions on activity vary in physical demand from walking to running on uneven ground. The LEFS is a validated tool and has demonstrated good test-retest reliability and responsiveness in individuals with persistent knee pain.

Secondary

MeasureTime frameDescription
Change in Patient Specific Functional Scale over timeBaseline, week 3 and week 15
Change in Musculoskeletal Health Questionnaire (MSK-HQ) over timeBaseline, week 3 and week 15
Change in Tampa Scale of Kinesiophobia (TSK) over timeBaseline, week 3 and week 15
Health Anxiety Depression Scale (HADS)Baseline
Change in International Physical Activity Questionnaire (IPAQ) over timeBaseline, week 3 and week 15
Change in Numeric Pain Rating Scale (NPRS) over timeBaseline, week 3 and week 15
Change in Sport Injury Rehabilitation Beliefs Survey (SIRBS) over timeBaseline, week 3 and week 15
Change in functional Activity Assessment (FAA) over timeBaseline and week 15
Change in five Repetition Maximum Leg Press over timeBaseline, week 3 and week 15
Change in isometric muscle strength of hip and knee using hand-held dynamometer over timeBaseline, week 3 and week 15
Change in single leg heel raises to fatigue over timeBaseline, week 3 and week 15
Change in qualitative assessment of single leg squat (QASLS) over timeBaseline, week 3 and week 15
Change in decline knee bend over timeBaseline, week 3 and week 15
Change in isometric midthigh pull over timeBaseline, week 3 and week 15
Change in Knee Injury and Osteoarthritis Outcome Score (KOOS) over timeBaseline, week 3 and week 15
Change in knee extension and flexion - maximal isometric voluntary contraction over timeBaseline, week 3 and week 15
Change in muscle volume and anatomical cross sectional area (CSA) using magnetic resonance imaging (MRI) over timeBaseline, week 3 and week 15
Change in pennation angle over time using ultrasonographyBaseline, week 3 and week 15Pennation angle measured in degrees
Change in fascicle length over time using ultrasonographyBaseline, week 3 and week 15fascicle length measured in mm
Change in single leg squat over time - kinetic and kinematic analysisBaseline, week 3 and week 153D motion capture and force plate data will be used to collect kinetic and kinematic data which will be later analysed using inverse dynamics. Force measured in Newtons, Moments measured in Newton/Metres/kg
Change in bilateral squat over time - kinetic and kinematic analysisBaseline, week 3 and week 153D motion capture and force plate data will be used to collect kinetic and kinematic data which will be later analysed using inverse dynamics. Force measured in Newtons, Moments measured in Newton/Metres/kg
Change in markers of muscle damage over timeBaseline, week 3 and week 15Using fasted blood samples. E.g., Creatine Kinase (units/L)
Change in markers of oxidative stress over timeBaseline, week 3 and week 15Using fasted blood samples. E.g., Protein carbonyl (units/L)
Change in markers of inflammation over timeBaseline, week 3 and week 15Using fasted blood samples. E.g., Interleukin-6 (pg/ml)
Change in markers of endothelial function over timeBaseline, week 3 and week 15Using fasted blood samples. E.g., Vascular endothelial growth factor (µg/L)
Change in daily monitoring of wellness score over timeDaily for the 3 weeks of rehabilitationSubjective patient reported outcome measure of 'wellness' scored using a 5-point likert scale.
Change in daily monitoring of session rate of perceived exertion (sRPE) over timeDaily for the 3 weeks of rehabilitationSubjective patient reported outcome measure of exertion, scored 0 to 10 (0 = no exertion, 10= maximal exertion)
Change in daily monitoring of pain over timeDaily for the 3 weeks of rehabilitationSubjective patient reported outcome measure of pain measured using a 0 to 100mm visual analog scale (VAS). 0= no pain, 100 = worst pain
Change in counter-movement jump over timeBaseline, week 3 and week 15

Countries

United Kingdom

Contacts

Primary ContactPeter Ladlow, PhD
peter.ladlow100@mod.gov.uk+44 (0)1509251500
Backup ContactRuss Coppack, PhD
Russ.Coppack100@mod.gov.uk+44(0)1509251500

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026