- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07575126
Comparison of Qigong and Otago in Patient With Diabetic Neuropathy
Comparison of Qigong and Otago on Agility, Balance, Gait, and Quality of Life in Patients With Diabetic Neuropathy
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Muneeb khan, PhD
- Phone Number: +92336799611
- Email: muneeb.khan@riphah.edu.pk
Study Locations
-
-
Punjab Province
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Guiranwala, Punjab Province, Pakistan, 54500
- DHQ Gujranwala
-
Contact:
- Javeria Ghazal, MS
- Phone Number: +923335154664
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Principal Investigator:
- Junaid Raza, MS
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Physician-diagnosed type 2 diabetes without gender bias, with peripheral neuropathy (defined by Michigan Neuropathy Screening Instrument questionnaire score of 5 or greater)
- Type 2 diabetic peripheral neuropathy patients
- The ability to walk independently for 10 m
- Having score between 46 to 52 (out of a total of 56 points) on the BBS
Exclusion Criteria:
- Fracture of the lower limb within the 6 months before the study (15)
- Diabetic ulcer, infection or partial amputation in feet (15)
- Disease or functional impairment of auditory, vestibular system (16)
- Any other medical conditions that would confound assessment of neuropathy such as malignancy, other neurological or orthopedic impairments (such as stroke, poliomyelitis, rheumatoid arthritis, prosthesis, or severe osteoarthritis), major vascular complications (venous or arterial ulcers), severe retinopathy, or severe nephropathy that causes edema or needs hemodialysis (17)
- Dementia or inability to give consistent information (18)
- History of surgical procedure at the knee, ankle, or hip or indication of surgery throughout the intervention period
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Qigong Balance
|
Quigong Balance Exercises 3 times per week for 60 minutes per session Open the Flow: Focus on fluid arm movements to enhance relaxation and improve circulation. Shaking Exercise: A full-body shake to release tension and promote energy flow. Lifting the Ball: Alternating arm movements simulating lifting a ball to improve upper body strength and coordination. Playing with Water: Slow, flowing movements that enhance balance and mindfulness. Weight Shifting and Balance Exercises: Stand with feet hip-width apart, shifting weight slowly from one leg to the other, holding each position for 10-15 seconds to engage stabilizing muscles in the legs and improve proprioception. Leg Lifts and Extensions: Perform controlled leg lifts (front, side, and back) to strengthen the quadriceps, hamstrings, and hip abductors. |
|
Active Comparator: Otago Balance
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Otago (Strengthening) Balance: Sit-to-stand exercises: to improve leg strength. Heel raises: to enhance calf strength. Toe stands: for improving foot stability. Balance Training: Single-leg stands: to enhance balance. Tandem walking: along a straight line. Side leg raises: to strengthen hip muscles 3 times per week for 60 minutes per session |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Agility T-Test
Time Frame: 12th week
|
The Agility T-Test is a performance-based assessment that measures an individual's agility and ability to change direction quickly.
It involves a sequence where the participant runs to a designated point, makes sharp turns around markers in a T-shaped layout, and returns to the starting position.
|
12th week
|
|
Berg Balance Scale
Time Frame: 12th week
|
is the gold standard test for static and dynamic balance abilities.
The BBS is used to measure ability to maintain balance while doing functional task search as reach, standing position and transferences.
It is a valid instrument used for the evaluation of effectiveness of interventions with quantitative description of function in clinical practice as well as research.
It consists of 14 items including simple balance tasks from everyday life.
|
12th week
|
|
Functional Reach Test
Time Frame: 12th week
|
FRT is a single item test for dynamic balance and acts as a quick screen for balance problems in older adults.
The distance between the lengths of an outstretched arm in a maximal forward reach, while maintaining a fixed base of support is measured.
A score of 6 inches or less indicates a significant increased risk for falls.
A score between 6-10 inches indicates a moderate risk for falls.
the Functional Reach Test (FRT) demonstrates an ICC of approximately 0.85 to 0.94
|
12th week
|
|
Gait Speed Test
Time Frame: 12th week
|
The Gait Speed Test measures the time it takes for an individual to walk a specific distance, usually 10 meters, at their usual pace.
It has demonstrated strong validity and reliability, with an Intra class Correlation Coefficient (ICC) often exceeding 0.90
|
12th week
|
|
10-Meter Walk Test
Time Frame: 12th week
|
The 10-Meter Walk Test involves timing a participant as they walk a distance of 10 meters at their comfortable pace.
It assesses gait speed, which is an important indicator of mobility and overall functional ability.
|
12th week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Javeria Ghazal, MS, Riphah International University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR &AHS/24/0297
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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