Skip to content

Home-based trunk intervention training to improve rigidity and functionality in people with Parkinson's disease

Home-based trunk intervention training to improve axial rigidity and functionality during activities of daily living in people with Parkinson's disease: a randomised clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14779929
Enrollment
18
Registered
2025-07-08
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Parkinson's disease Nervous System Diseases

Interventions

1. Trunk-targeted exercise programme 2. General exercise programme Treatments will be administered using a single-blind matched-pairs design. Participants will undergo either trunk-targeted exercise

Sponsors

University of Kent
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed with idiopathic Parkinson's disease 2. Classified between stage I-IV on Hoehn and Yahr (H&Y) classification scale during the clinical 'ON' state 3. Able to understand simple motor commands and of adequate cognition (screened using the Montreal Cognitive Assessment [MoCA]) 4. Able to walk 10 m without assistance 5. Regular use of and no change in antiparkinsonian medication in the last month 6. Aged 40-80 years

Exclusion criteria

Exclusion criteria: 1. Previously had deep-brain stimulation (DBS) surgery. 2. Presented with comorbidities that may affect movement patterns. 3. Presented with comorbidities that may affect their capacity to exercise. 4. Changed their medication type and/or dosage throughout the duration of the study. 5. Score poorly on the Falls Risk Assessment Tool (FRAT) and Falls Efficacy Scale - International (FES-I) assessment for fall risk. 6. Score poorly on the MoCA. 7. Investigator's determination of unsuitability for trial participation.

Design outcomes

Primary

MeasureTime frame
Axial rigidity measured using 3D motion capture at baseline, 4, 8, 12 and 24 weeks

Secondary

MeasureTime frame
1. Gait kinematics measured using 3D motion capture at baseline, 4, 8, 12 and 24 weeks 2. Functionality measured using Timed-Up and Go (TUG), Functional Reach Test (FRT), Berg Balance Scale (BBS) and Five-Times Sit to Stand Test (FTSST) at baseline, 4, 8, 12 and 24 weeks 3. Postural balance during 30-second quiet stand using 3D motion capture at baseline, 4, 8, 12 and 24 weeks

Countries

England, United Kingdom

Contacts

Public ContactLewis Ball
lrb33@kent.ac.uk+44 (0)1227 764000

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026