Wrist Heavy Slow Resistance and Shoulder Stabilization Exercises on Pain, Grip Strength and Functional Ability in Lateral Epicondylitis
Comparative Impact of Wrist Heavy Slow Resistance and Shoulder Stabilization Exercises on Pain, Grip Strength and Functional Ability in Lateral Epicondylitis
1 other identifier
interventional
32
1 country
1
Brief Summary
The study will compare the shoulder and wrist treatment approaches to determine their effect on elbow. Thirty-two medically stable participants with active shoulder and wrist movements will be enrolled into two groups. Both groups will receive structured training for six weeks. Outcomes will be measured using standardized assessment tools. The aim is to identify the more effective strategy for improving upper limb kinetic chain which is affected by lateral epicondylitis
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 2, 2026
CompletedFirst Submitted
Initial submission to the registry
May 4, 2026
CompletedFirst Posted
Study publicly available on registry
May 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 2, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 2, 2026
May 8, 2026
May 1, 2026
4 months
May 4, 2026
May 4, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Pain
Pain will be measured with the help of Numeric Pain Rating Scale (NPRS). This scale is validated to measure the pain in both upper and lower limb.
Six weeks
Secondary Outcomes (1)
Grips strength and Functional Ability
Six weeks
Study Arms (2)
Group A: Wrist heavy slow resistance exercises with hot pack.
EXPERIMENTALHot pack applied to target muscles (depending on requirement of patient like wrist and finger extensors) with 15-20 minutes duration Treatment: Wrist heavy slow resistance exercises performed with the help of weights by stabilizing the hand on the table. As the repetitions will got increased, as the weight will decrease. Sessions conducted 3 times/week for 6 weeks.
Group B: Shoulder stabilization exercises with hot pack.
ACTIVE COMPARATORHot pack applied to target muscles (depending on requirement of patient like shoulder stabilizers) with 15-20 minutes duration Treatment: This trial include the shoulder stabilization exercises performed with the help of theraband by stabilizing the subject across the wall and check the effect on elbow to treat lateral epicondylitis. Sessions conducted 3 times/week for 6 weeks.
Interventions
Wrist heavy slow resistance exercises performed with the help of weights by stabilizing the hand on the table. As the repetitions will got increased, as the weight will decrease. Sessions conducted 3 times/week for 6 weeks.
This trial include the shoulder stabilization exercises performed with the help of thera-band by stabilizing the subject across the wall and check the effect on elbow to treat lateral epicondylitis
Eligibility Criteria
You may qualify if:
- Both genders will be involved with ages 30-50. Patients who have had pain for the last 2 weeks with tenderness. Subjects who will have a positive cozen test. Also include those who have a radiological graph with normal bone and joint alignment of the upper limb.
- Include those who will be clinically diagnosed with LE from the orthopedic OPD. A pain score of more than or equal to 4 in NPRS diagnosed as tennis elbow.
You may not qualify if:
- Those who will have pain on the lateral aspect of the elbow for 6 months or more than 6 months.
- Subjects who will be diagnosed with cervical radiculopathy. Those who will have the injury and disease around the shoulder, elbow and wrist.
- Those with a history of elbow surgery, open wound and infectious limb. Those with a history of rheumatoid arthritis and osteoarthritis. Those who have any fracture of the treatment side upper limb. systemic illness like bleeding disorders, anticoagulants, diabetes, and hypertension.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pulse Hospital
Sādiqābād, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
May 4, 2026
First Posted
May 8, 2026
Study Start
February 2, 2026
Primary Completion (Estimated)
June 2, 2026
Study Completion (Estimated)
June 2, 2026
Last Updated
May 8, 2026
Record last verified: 2026-05