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Clinical Trials/NCT06428123
NCT06428123Active, not recruitingNot Applicable

Comparison of Efficacy of Mirror Therapy vs Mental Imagery in Reduction of Phantom Limb Pain in Above Knee Amputee Patients: A Comparative Study

Superior University2 sites in 1 country24 target enrollmentStarted: November 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
24
Locations
2
Primary Endpoint
The Numeric Rating (NRS)

Study Overview

Brief Summary

Limb amputation results in many types of pain, including localized pain at the stump and projected pain experienced by the patient in the location where the amputated limb used to be, known as phantom limb pain (PLP). The aim of this study is to determine the relative benefits of mirror therapy vs mental imagery in reduction of phantom limb pain. Randomized clinical trial study design will be followed.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
12 Years to 75 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Both male and female gender with ages from 12 to 75 years (17).
  • •Individuals with a unilateral above-knee amputation (AKA) at least 6 months prior to the study.
  • •Experiencing phantom limb pain at least 3 months (16).

Exclusion Criteria

  • •History of neurological disorders affecting pain perception or motor function (e.g., stroke, spinal cord injury, brain injury).
  • •Uncontrolled diabetes or other medical conditions that could affect healing or participation in the study.
  • •Pregnancy or breastfeeding.

Arms & Interventions

Mental Imagery

Other

Intervention: Mental Imagery on present Lower Limb (Diagnostic Test)

Mirror Therapy

Experimental

Intervention: Mirror Therapy on present Lower Limb (Behavioral)

Outcomes

Primary Outcomes

The Numeric Rating (NRS)

Time Frame: 12 Months

it is a simple and widely used tool for measuring pain intensity. It consists of a horizontal line with 11 numbered points, ranging from 0 (no pain) to 10 (worst pain imaginable). Patients are asked to rate their pain by selecting the number that best describes their current pain intensity

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Study Sites (2)

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