The effect of rehabilitation on patients with carpal tunnel syndrome after surgery

The effect of rehabilitation interventions based on the patient's condition, on the sensation, function and pain of patients with carpal tunnel syndrome after surgery

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017041233390N1

Enrollment

Registered

2017-07-07

Start date

2016-01-19

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Carpal Tunnel Syndrome. Carpal Tunnel Syndrome

Interventions

Intervention 1: Intervention group receives rehabilitation treatment (the early motion), depending on the patient condition, this rehabilitation, depending on the patient include scar reduction techn

Rehabilitation

Intervention group receives rehabilitation treatment (the early motion), depending on the patient condition, this rehabilitation, depending on the patient include scar reduction techniques, standard

The control group (dressing) do not receives any intervention. Actually this group recieves routine post-operative care such as dressing and recommendations for action, according to the doctor.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with carpal tunnel syndrome is diagnosed by a specialist and NCV test and Phalen tests and tinnel sign be positive; patients with idiopathic CTS; people who do not experience trauma and ankle injuries or have not had previous surgery. Exclusion criteria: Injury or trauma during intervention; double Crush Syndrome; certain diseases such as rheumatoid arthritis, autoimmune and metabolic disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Visual Analogue Scale.;Sensation. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Semmes Weinstein Test of Monofilaments.;Function. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Boston Questionnaire(function section).;Hand power(tip pinch, key pinch, grip). Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Vigorimeter.	—

Measure

Time frame

Pain. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Visual Analogue Scale.;Sensation. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Semmes Weinstein Test of Monofilaments.;Function. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Boston Questionnaire(function section).;Hand power(tip pinch, key pinch, grip). Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Vigorimeter.

—

Secondary

Measure	Time frame
Symptoms. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Boston Questionnaire(symptoms section).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoya Mahmoodi

The University of Social Welfare and Rehabilitation Sciences

royamahmoodi95@yahoo.com+98 21 2218 0037

Outcome results

None listed

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