Skip to content

A1 Pulley Stretching Along With Tendon Gliding Exercises in Post-operative Patients of Trigger Finger

Synergistic Effects of A1 Pulley Stretching Along With Tendon Gliding Exercises on Pain, Range of Motion, and Hand Grip Strength in Post-operative Patients of Trigger Finger.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07482397
Enrollment
30
Registered
2026-03-19
Start date
2025-01-13
Completion date
2025-10-31
Last updated
2026-03-19

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

Conditions

Trigger Finger

Keywords

Trigger finger, A1 pulley stretching, Tendon- glinding exercises, postoperative rehabilitation, Range of motion, Grip strength, Randomized controlled trial

Brief summary

The study was conducted to determine the synergistic effects of A1 pulley stretching along with tendon gliding exercises on pain, range of motion, and hand grip strength in post-operative patients of trigger finger

Interventions

OTHERA1 pulley stretching

Participants comfortably seated with the arm supported on a table. The right palm placed on the couch, and the middle fingers positioned alternately on a wooden block at a 45° angle. Participants flex the middle finger while the therapist provides resistance to induce an isometric contraction. Duration and Repetitions: * Each stretch: 15-30 seconds * 10 repetitions per session * sets with 30-60 seconds rest Frequency: Three times per week during therapy sessions

OTHERTendon Gliding exercises

5 glide × 3 sets: * Open Palm * Hook Fist * Tabletop * Half Fist * Full Fist Each glide is performed in a controlled, pain-free manner. Frequency: Three weekly supervised sessions.

Heat therapy gloves for 10 minutes TENS with frequency of 80-100 Hz at low intensity having pulse duration of 50-80μs for 10 minutes. Paraffin wax bath at 52 degree centigrade 10 times for 15 minutes a day.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
36 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Both gender male and female * Age 35 ≤ 60 * Patients with clear wound and removed stitched * Symptoms of locking finger for more than 6 months * Positive Hueston tabletop test * NPRS score of 4 to 7

Exclusion criteria

* Finger joint problem by joint fracture * Recent trauma * Presence of open wound, local infection * Known case of tumor * Congenital and autoimmune disorders

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating ScaleFrom enrollment to end of treatment 6 weeksNumeric Pain Rating Scale (NPRS) is used to determine the level of pain in a patient. It gives people an opportunity to self-report their pain levels using a scale of zero to ten, with 0 being the absence of pain and 10 being the worst that can happen. The scale is divided into categories, 1-3 mild pain, 4-6 moderate pain, and 7- 10 severe pain.
Universal GoniometerFrom enrollment to the end of treatment at 6 weeks.goniometer is a device that is widely utilized in orthopedics and physical therapy to estimate the range of motion of a joint (ROM) and to diagnose range restrictions.
Hand dynamometerFrom enrollment to the end of treatment for 6 weeks.A hand dynamometer is a tool that is used to measure the grip strength and give a quantitative measure of the muscle activity in the hand and forearm. Through pressing of the handle of the device, the user can measure the force used, and the clinicians can observe the progress and see the changes in the rehabilitation

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORHumera Mubashar

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026