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Effectiveness of coordinative locomotor training on pain, balance and gait in chemotherapy induced peripheral neuropathy patients

Effectiveness of coordinative locomotor training on pain, balance and gait in chemotherapy induced peripheral neuropathy patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240311061260N1
Enrollment
38
Registered
2024-05-03
Start date
2024-05-06
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Chemotherapy induced peripheral neuropathy. Other disorders of peripheral nervous system

Interventions

Intervention 1: Intervention group: Coordinative Locomotor Training group. Intervention 2: Control group: conventional training (Reaching out with hands crossed in sitting position, Sitting and gettin

Sponsors

The University of Faisalabad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 35 to 60 years Both genders male and female Willing to participate in research Cancer patients of stage ?-? Receiving neurotoxic drugs (platinum based, taxanes based or both in combination) Have received at least 4 cycles of chemotherapy treatment Having numbness and tingling in distal areas Pain in distal areas At medium (19-24) to high (<19) risk of fall according to POMA Able to communicate in Punjabi/Urdu/English

Exclusion criteria

Exclusion criteria: Cognitive dysfunction (Mini-Mental State exam score?24) Any recent major surgery Having diabetic neuropathy before getting chemotherapy drugs Unhealed lower extremity fracture Other neurological problems including brain cancer Cardiovascular diseases Bone metastasis Lower limb lymphedema Musculoskeletal problems Amputated limb With abnormal visual or auditory senses Uncooperative patients

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before treatment and at the end of 4 weeks of intervention. Method of measurement: Numerical pain rating scale(NPRS) was used.;Balance. Timepoint: Before the treatment and at the end of 4 weeks of intervention. Method of measurement: Performance oriented mobility assessment (POMA).;Gait. Timepoint: Before the treatment and at the end of 4 weeks of intervention. Method of measurement: Timed up and go test(TUG), F8WT(figure of 8 walk test).

Countries

Pakistan

Contacts

Public ContactAqsa Liaqat

The University of Faisalabad

aqsa786liaqat@gmail.com+92 335 7813723

Outcome results

None listed

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