ClinicalTrials.gg
RecruitingNCT07907302SARCOPARKINSONUpdated Oct 30, 2026

Strength and Dual-Task on Sarcopenia in People With Parkinson's Disease

An interventional study of Nutricional Education and General Exercise Guidelines and Progressive Resistance Training With Cognitive Dual-Task Training in PARKINSON DISEASE (Disorder) and Parkinsonism or Parkinson's Disease Nos, sponsored by University of Valencia. Recruiting at 1 site in Spain. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by University of Valencia · Not applicable, Interventional, and Treatment

Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

Study summary

Parkinson´s disease and parkinsonian syndromes are associated with progressive motor and non-motor impairments that may compromise functional independence and quality of life. Sarcopenia, characterized by reduced muscle strength, muscle mass, and physical performance, is highly prevalent in these populations and may contribute to an increased risk of falls, frailty, and disability.

This prospective, parallel-group, three-arm randomized controlled trial aims to compare the effects of three levels of physiotherapy intervention on sarcopenia-related parameters and physical function in adults with Parkinson´s disease or parkinsonian syndromes.

The Education Group will receive standarized nutritional education and general physical exercise recommendations through structed educational materials, without supervised exercise training. The Progressive Resistance Training (PRT) Group will receive standarized nutritional education and participate in supervised progressive resistance trained combined with cognitive dual-task exercises. The PRT plus Instability Group will receive the same nutritional education, progressive resistance training, and cognitive dual-task training, with additional instability and postural control components. Participants in the two supervised exercise groups will complete two physiotherapy sessions per week for 12 weeks.

Assessments will be conducted at baseline (T0), immediately after the 12-week intervention (T1), and four weeks after completion of the intervention (T2). Outcomes will include clinical and functional status, muscle strength, body composition and other sarcopenia-related measures, physical performance, nutritional status, neurocognitive status, number of falls, and Parkinson's disease-related clinical characteristics.

The study will evaluate the effects of supervised progressive resistance training compared with an educational intervention and will explore whether adding instability and postural control demands to progressive resistance training provides additional effects on physical function, sarcopenia-related outcomes, and fall-related functional risk in people with Parkinson's disease and parkinsonian syndromes.

Read the detailed description

Parkinson's disease (PD) and parkinsonian syndromes are neurodegenerative conditions characterized by progressive motor and non-motor impairments that can negatively affect functional independence and quality of life. In these populations, sarcopenia and reductions in muscle strength and physical performance may contribute to frailty, falls, disability, and loss of independence.

Progressive resistance training (PRT) represents a potentially relevant physiotherapy intervention for addressing muscle weakness and sarcopenia-related impairments in people with Parkinson's disease. Previous research has shown that resistance training can improve muscle strength and functional performance when appropriately prescribed and supervised. However, most available studies have focused primarily on idiopathic Parkinson's disease and have generally examined resistance training from a functional perspective rather than within a comprehensive sarcopenia framework integrating muscle strength, body composition, physical performance, nutritional status, and cognitive characteristics.

People with Parkinson's disease and parkinsonian syndromes may also experience difficulties when performing motor and cognitive tasks simultaneously. These dual-task difficulties can interfere with mobility and activities of daily living. Therefore, incorporating cognitive tasks into physical training may facilitate the assessment and training of cognitive-motor interaction within a functional context.

In addition, postural instability and impaired balance are clinically relevant features in Parkinson's disease and some parkinsonian syndromes. Resistance training performed with additional instability or postural control demands may provide a different stimulus from conventional progressive resistance training. Nevertheless, comparative evidence regarding progressive resistance training with and without instability remains limited.

Nutritional status may also influence sarcopenia and the response to exercise. For this reason, standardized nutritional education is incorporated into all three study groups, allowing the supervised exercise components to be compared while maintaining a common educational approach across interventions.

This study is designed as a prospective, parallel-group, three-arm randomized controlled trial involving adults with a clinical diagnosis of Parkinson's disease or parkinsonism confirmed by a neurologist. Participants must be aged 18 years or older, be classified within Hoehn and Yahr stages 1-3, have stable antiparkinsonian medication for at least four weeks, be able to ambulate independently with or without an assistive device, and be able to understand and follow basic safety instructions.

Participants with severe or uncontrolled additional pathology, other neurological diseases that interfere with assessment, recent fractures, severe dyskinesias or unpredictable motor fluctuations that compromise safety, or medical conditions contraindicating supervised physical exercise will be excluded.

Following the baseline assessment, eligible participants will be randomly assigned to one of three intervention groups:

Education Group: Participants will receive standardized nutritional education and general physical exercise recommendations according to usual clinical recommendations for people with Parkinson's disease. The intervention will include an initial face-to-face session in which structured educational materials will be explained and provided. A follow-up session will be conducted midway through the 12-week intervention period to answer questions, reinforce the recommendations included in the educational materials, and review adherence to the proposed nutritional and exercise guidelines. Participants in this group will not participate in structured strength training or supervised exercise sessions as part of the study.

Progressive Resistance Training (PRT) Group: Participants will receive standardized nutritional education and a supervised progressive resistance training program targeting the lower limbs, upper limbs, and trunk muscles. Exercises will use dumbbells, resistance bands, weights, body weight, and other appropriate therapeutic exercise resources. Training intensity will be individually adjusted and progressively increased toward approximately 60%-90% of one-repetition maximum (1-RM), according to each participant's functional status, exercise tolerance, and progression. Training load will be periodically adjusted by modifying the external resistance or exercise complexity. Cognitive dual tasks will be simultaneously incorporated into the exercise program to address cognitive-motor interference and promote functional transfer.

Progressive Resistance Training plus Instability (PRT + Instability) Group: Participants will receive the same standardized nutritional education, progressive resistance training, and cognitive dual-task components as the PRT Group. The relative training intensity and strength-training load will follow the same principles as those used in the PRT Group. In addition, instability and increased postural control demands will be incorporated through unstable surfaces and other postural challenges. Exercise intensity and complexity will be individually adapted according to each participant's functional and cognitive status, with safety and adherence prioritized throughout the intervention.

Participants allocated to the PRT and PRT + Instability groups will complete two supervised physiotherapy sessions per week for 12 weeks. Sessions will be supervised by a physiotherapist and individualized according to the participant's abilities, functional status, cognitive status, exercise tolerance, and clinical presentation.

Study assessments will be conducted at three time points: baseline before the intervention (T0), immediately following completion of the 12-week intervention (T1), and four weeks after completion of the intervention (T2). This design will allow the evaluation of within-group and between-group changes and the initial persistence of intervention effects following completion of supervised training.

Clinical and functional assessment will include the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS Parts I-IV), fall recording, the Short Physical Performance Battery (SPPB), and the Timed Up and Go (TUG). Neurological diagnosis, relevant clinical characteristics, dopaminergic medication, ON/OFF status, levodopa equivalent daily dose (LEDD), available neuroimaging, and relevant clinical history will be recorded at baseline and updated at subsequent assessments when clinically relevant changes occur.

Sarcopenia-related assessment will follow the conceptual framework of the European Working Group on Sarcopenia in Older People (EWGSOP2). Measures will include SARC-F, calf circumference, handgrip dynamometry, physical performance assessment, and body composition measured using bioelectrical impedance analysis.

Nutritional status will be assessed using the Mini Nutritional Assessment-Short Form (MNA-SF) and the Malnutrition Screening Tool (MST). The EAT-10 questionnaire will also be used to screen for self-reported swallowing difficulties.

Neurocognitive status will be classified according to DSM-5 criteria as normal cognition, mild neurocognitive disorder, or major neurocognitive disorder. Neurocognitive status will be considered as part of the multimodal characterization of participants and as a potential factor influencing treatment response and tolerance to cognitive-motor dual-task training. Neurocognitive reassessment will also be performed at post-intervention and follow-up assessments according to neuropsychological criteria.

The Charlson Comorbidity Index will be recorded as part of the baseline clinical characterization. When available from participants' medical records or routine clinical practice, analytical biomarkers including vitamin D, albumin/prealbumin, hemoglobin, hematocrit, total cholesterol, HDL cholesterol, and LDL cholesterol will also be recorded. No blood tests will be specifically performed for the purpose of obtaining these biomarkers for the study.

Available neuroimaging information, including DaTSCAN, PET-DOPA, and brain magnetic resonance imaging, will be recorded when available in the clinical record. New neuroimaging or analytical information arising during the study may be incorporated into subsequent assessments when clinically relevant. These medical examinations are not performed specifically as part of the study intervention.

The interventions are based on therapeutic exercise and strength-training procedures commonly used in clinical practice. Potential intervention-related risks are considered low and may include transient muscle discomfort, fatigue, dizziness, musculoskeletal pain, or imbalance during exercise. To minimize these risks, supervised sessions will be individually adapted and will follow principles of progressive loading, safety, and adequate recovery.

If an adverse event occurs during an intervention session, exercise will be stopped immediately and the participant will be assessed by the healthcare professional responsible for the intervention. Appropriate clinical follow-up will be provided according to the nature and severity of the event, including referral to medical or healthcare services when required. Adverse events will be recorded and documented, including their severity, evolution, and possible relationship with the intervention. Continued participation will be considered individually according to clinical safety criteria.

The main objective of the trial is to compare the effects of the three intervention approaches-education, progressive resistance training with cognitive dual tasks, and progressive resistance training with cognitive dual tasks plus instability-on sarcopenia-related parameters and physical function in people with Parkinson's disease and parkinsonian syndromes.

Secondary objectives include describing participants' neurocognitive and nutritional profiles and their sarcopenia and physical-function characteristics; analyzing changes in muscle strength, body composition, and functional performance associated with each intervention; evaluating the effects of incorporating instability on postural control and fall-related functional risk; and exploring the potential influence of neurocognitive and nutritional status on response to treatment.

By comparing these three clinically applicable intervention approaches, the study aims to provide further evidence regarding the role of progressive resistance training within a multimodal approach to sarcopenia and functional impairment in people with Parkinson's disease and parkinsonian syndromes, as well as the potential additional contribution of instability and postural control demands.

02

Conditions studied

  • PARKINSON DISEASE (Disorder)
  • Parkinsonism or Parkinson's Disease Nos

Keywords

  • Parkinson's disease
  • Parkinsonism
  • Progressive resistance training
  • Strength training
  • Dual-task training
  • Instability resistance training
  • Sarcopenia
  • Muscle strength
  • Physical function
  • Postural control
  • Fall risk
  • Cognitive-motor interference
  • Nutritional status
03

In context

Parkinson Disease

4,573 studies on the registry are indexed under Parkinson Disease; 1,086 are open to participants now.

This study's planned enrollment of 60 is above the median of 40 across 3,353 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

University of Valencia is the lead sponsor of 357 studies on the registry; 75 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Clinical diagnosis of Parkinson's disease or parkinsonism confirmed by a neurologist.
  • Hoehn and Yahr stage 1-3.
  • Age ≥18 years.
  • Stable antiparkinsonian drug treatment for at least the previous 4 weeks.
  • Ability to ambulate independently, with or without assistive devices.
  • Ability to understand and follow basic safety instructions.

Exclusion criteria

Exclusion Criteria:

  • Severe or uncontrolled additional pathology.
  • Other neurological diseases that interfere with the assessment.
  • Recent fractures.
  • Severe dyskinesias or unpredictable motor fluctuations that compromise safety.
  • Any medical condition that contraindicates supervised physical exercise
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Education group

    Participants will receive standardized nutritional education and general physical exercise guidelines through structured educational materials in a strucutred way throughout 12-weeks.

    Behavioral: Nutricional Education and General Exercise Guidelines

  • Experimental
    Progressive Resistance Training (PRT)

    Participants will receive standardized nutritional education and progressive resistance training combined with cognitive dual-task training by mean of two supervised physiotherapy sessions per week for 12 weeks.

    Behavioral: Progressive Resistance Training With Cognitive Dual-Task Training

  • Experimental
    Progressive Resistance Training + Inestability Group

    Participants will receive standardized nutritional education and the same progressive resistance and cognitive dual-task training principles as the PRT Group, with the addition of instability and increased postural control demands, 2 sessions per week for 12 weeks.

    Behavioral: Progressive Resistance Training With Cognitive Dual-Task and Inestability Training

Interventions

  • BehavioralNutricional Education and General Exercise Guidelines

    Participants will receive standardized nutritional education and general physical exercise guidelines through a structured information booklet. An initial face-to-face session will be conducted to explain the educational materials and recommendations. A second face-to-face follow-up session will be held midway through the 12-week intervention period to answer questions, reinforce the recommendations, and review adherence to the proposed nutritional and exercise guidelines. No structured strength training or supervised exercise sessions will be provided as part of this intervention.

  • BehavioralProgressive Resistance Training With Cognitive Dual-Task Training

    Participants will receive standardized nutritional education and complete a 12-week supervised progressive resistance training program combined with cognitive dual-task training. Training will be performed twice weekly and will target the lower limbs, upper limbs, and trunk using dumbbells, resistance bands, weights, and bodyweight exercises. Training intensity will be individually adjusted and progressively increased toward 60%-90% of one-repetition maximum (1-RM). Training load will be periodically adjusted according to participant progression. Cognitive tasks will be performed simultaneously with physical exercises to address cognitive-motor interference.

  • BehavioralProgressive Resistance Training With Cognitive Dual-Task and Inestability Training

    Participants will receive standardized nutritional education and complete a 12-week supervised progressive resistance training program combined with cognitive dual-task training and instability components. Training will be performed twice weekly and will target the lower limbs, upper limbs, and trunk. The same relative strength-training intensity and load principles as the PRT intervention will be applied. Additional instability and postural control demands will be incorporated through unstable surfaces and other postural challenges. Training intensity and complexity will be individually adapted according to functional and cognitive status.

06

What researchers measure

Primary outcomes

  1. Handgrip Strength

    Handgrip strength will be assessed using handgrip dynamometry as a measure of muscle strength within the EWGSOP2 sarcopenia assessment framework. Higher values indicate greater muscle strength.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  2. Physical Performance - Short Physical Performance Battery (SPPB)

    Physical performance will be assessed using the Short Physical Performance Battery (SPPB), which evaluates balance, gait speed, and lower-limb functional performance. The total score ranges from 0 to 12 points, with higher scores indicating better physical performance.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  3. Body Composition -Body fat (%)

    It will be assessed assessed using bioelectrical impedance analysis (BIA) , measured in %.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  4. Body Composition -Body fat (kg)

    It will be assessed assessed using bioelectrical impedance analysis (BIA), measured in kg.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  5. Body Composition -Lean mass (kg)

    It will be assessed assessed using bioelectrical impedance analysis (BIA) , measured in kg.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  6. Body Composition -Lean mass (%)

    It will be assessed assessed using bioelectrical impedance analysis (BIA) , measured in %.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  7. Body Composition -body water(%)

    It will be assessed assessed using bioelectrical impedance analysis (BIA) , measured in %.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  8. Body Composition -body water(kg)

    It will be assessed assessed using bioelectrical impedance analysis (BIA) , measured in kg.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

Secondary outcomes

  1. Functional Mobility - Timed Up and Go (TUG)

    Functional mobility will be assessed using the Timed Up and Go (TUG) test. The time required to stand up from a chair, walk 3 meters, turn, walk back, and sit down will be recorded in seconds. Lower completion times indicate better functional mobility.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  2. Sarcopenia Risk - SARC-F

    Sarcopenia risk will be assessed using the SARC-F questionnaire, which evaluates strength, assistance with walking, rising from a chair, climbing stairs, and falls. The total score ranges from 0 to 10 points, with higher scores indicating greater risk of sarcopenia.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  3. Calf Circumference

    Calf circumference will be measured as an anthropometric indicator related to muscle mass and sarcopenia. Measurements will be recorded in centimeters, with higher values indicating greater calf circumference.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  4. Parkinson's Disease Severity - Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS)

    Parkinson's disease-related motor and non-motor symptoms will be assessed using the MDS-UPDRS Parts I-IV. The scale evaluates non-motor experiences of daily living (Part I), motor experiences of daily living (Part II), motor examination (Part III), and motor complications (Part IV). Higher scores indicate greater disease-related impairment or severity.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  5. Number of Falls

    Falls occurring during the study period will be recorded as part of the clinical and functional assessment. The number of falls reported by each participant will be documented, with a higher number indicating a greater occurrence of falls.

    Time frame: Baseline (T0), throughout the 12-week intervention period, and at the 4-week post-intervention follow-up (T2).

  6. Nutritional Status - Mini Nutritional Assessment-Short Form (MNA-SF)

    Nutritional status will be assessed using the Mini Nutritional Assessment-Short Form (MNA-SF). The total score ranges from 0 to 14 points, with higher scores indicating better nutritional status and lower scores indicating greater risk of malnutrition.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  7. Malnutrition Risk - Malnutrition Screening Tool (MST)

    Risk of malnutrition will be assessed using the Malnutrition Screening Tool (MST), which considers recent unintentional weight loss and reduced food intake related to decreased appetite. Higher scores indicate greater risk of malnutrition.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  8. Self-Reported Swallowing Difficulties - Eating Assessment Tool-10 (EAT-10)

    Self-reported swallowing difficulties will be assessed using the Eating Assessment Tool-10 (EAT-10), a 10-item questionnaire evaluating symptoms related to swallowing. The total score ranges from 0 to 40 points, with higher scores indicating greater self-perceived swallowing difficulties.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

  9. Neurocognitive Status According to DSM-5 Criteria

    Neurocognitive status will be clinically classified according to DSM-5 criteria into one of three categories: normal cognition, mild neurocognitive disorder, or major neurocognitive disorder. Neurocognitive classification will be used to characterize participants and explore its potential influence on response to the intervention and tolerance to cognitive-motor dual-task training.

    Time frame: Baseline (T0), immediately after the 12-week intervention (T1), and 4 weeks after intervention completion (T2).

07

Study locations

1 of 1 sites recruiting
  • Clínica NYR
    Valencia, Valencia 46015, Spain
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) are not currently planned to be shared publicly or with other researchers, as no specific IPD-sharing plan has been established for this study. Participant data will be handled in accordance with the approved study protocol, informed consent procedures, and applicable data protection requirements. Any future sharing of anonymized data for research purposes would be subject to appropriate ethical and data protection requirements.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jan 2027; primary completion for Jan 2027, 0 months later.

Of 1,291 non-industry interventional studies with no phase under Parkinson Disease, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 44. This study's planned 0 months is below that.

Counting every sponsor, half of 1,367 studies reached it within 25 months; a quarter within 11 and three quarters within 44.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 15, 2026
First posted
Oct 30, 2026
StartEst.
Jan 11, 2027
Primary completionEst.
Jan 29, 2027
CompletionEst.
Dec 31, 2031
Last update
Oct 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07907302
Collaborators
CLÍNICA NYR - INSTITUTO VALENCIANO DE NEUROLOGÍA
Responsible party
Anna Arnal Gómez, PhD (Senior Lecturer in Physiotherapy, University of Valencia) — Principal investigator
First posted
Oct 30, 2026
Start date
Jan 11, 2027 (estimated)
Primary completion
Jan 29, 2027 (estimated)
Completion
Dec 31, 2031 (estimated)
Last update
Oct 30, 2026

Study contacts

Anna Arnal Gómez, PhD
Contact
anna.arnal@uv.es
+34 963983853 ext. 51227
Ana Santamaría Balfagón, PT
Contact
asanbal@alumni.uv.es
+ 34 633 133 196
Anna Arnal Gómez, PhD
principal investigator · Department of Physiotherapy, University of Valencia
Maria Damià Vidal, PhD
study director · CLÍNICA NYR - INSTITUTO VALENCIANO DE NEUROLOGÍA

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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