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evaluating the impact of exercise protocol called rhythmic amplitude motor progression on diabetic patients who have neuropathy to evaluate their balance and walking pattern

Evaluating the Impact Rhythmic-Amplitude Motor Progression (RAMP) Protocol on Gait, Balance, Endurance, and Functional Mobility in Individuals with Diabetic Peripheral Neuropathy:A Multicentric Double-Blind Randomized Controlled Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101268
Enrollment
66
Registered
2026-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: E114- Type 2 diabetes mellitus with neurological complications

Interventions

Intervention1: intervention group:Rythmic amplitude motor progression training Control group:Conventional Physiotherapy: to the intervention group Rhythmic-Amplitude Motor Progression (RAMP) is a 6w

Sponsors

college of physiotherapy,Dayananda sagar university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants will include individuals who are currently on medication for diabetes. Eligible participants must present sensory impairment with an MNSI score of equal or more 2.5 points and have the ability to walk household distances without assistance. Additionally, participants should have ankle muscle power greater than MRC grade 3 and a Berg Balance Scale (BBS) score of more than 21.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they have a foot ulcer at the time of intake, any orthopedic condition that influences gait, or neurological problems other than diabetic peripheral neuropathy. Individuals with vestibular disorders, diabetic retinopathy, or middle ear infections that may affect balance or gait will also be excluded. Additionally, patients with uncontrolled cardiovascular or respiratory disorders will not be eligible to participate.

Design outcomes

Primary

MeasureTime frame
10MWT BBS 6MWTTimepoint: Pre and Post intervention

Secondary

MeasureTime frame
ABC TUG DGITimepoint: Pre and Post intervention

Countries

India

Contacts

Public ContactSUNJYOTH H S

college of physiotherapy , Dayananda Sagar University

sanjyoth05@gmail.com8722555859

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026