- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07415174
Neck Exercises After Thyroid Surgery
February 15, 2026 updated by: Mertcan AK, Istanbul University - Cerrahpasa
Effect of Postoperative Neck Range-of-Motion and Isometric Strengthening Exercises on Neck Pain and Early-Stage Quality of Life After Thyroidectomy
Postoperative neck pain is common after thyroidectomy and may impair early recovery.
This prospective randomized controlled study aimed to evaluate the effects of postoperative neck range-of-motion (ROM) and isometric strengthening exercises on neck pain and early-stage quality of life in patients undergoing thyroidectomy.
Between November 2024 and April 2025, 93 patients who underwent thyroidectomy were enrolled.
Surgical indications included multinodular goiter, Graves' disease, and fine-needle aspiration biopsy results classified as Bethesda categories III-VI.
Patients were randomized into an intervention group (n = 48) and a control group (n = 45).
Patients in the intervention group performed cervical ROM and isometric strengthening exercises from postoperative day 1 to day 10, while the control group received standard postoperative care without a structured exercise program.
Both groups were evaluated on postoperative days 1 and 10.
Pain severity was assessed using the Visual Analog Scale (VAS), and quality of life was assessed using the Neck Pain, Discomfort, and Early-Stage Quality of Life Questionnaire (NPDEPQ).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
93
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Istanbul
-
Istanbul, Istanbul, Turkey (Türkiye), 34096
- Istanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, Department of General Surgery
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Adults aged 18 years or older
- Patients who underwent thyroidectomy for multinodular goiter, Graves' disease, or fine-needle aspiration biopsy results classified as Bethesda categories III, IV, V, or VI
- Ability to understand and comply with the study protocol
- Provision of written informed consent
Exclusion Criteria:
- Age younger than 18 years
- History of previous neck surgery
- Cervical disc herniation
- Parathyroidectomy
- Hashimoto's thyroiditis
- Refusal to provide written informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Postoperative Neck Exercise Program
Patients received a structured postoperative neck range-of-motion and isometric strengthening exercise program in addition to standard postoperative care.
|
A structured postoperative program including neck range-of-motion and isometric strengthening exercises, initiated on postoperative day 1 and performed for 10 consecutive days, three times daily.
|
|
No Intervention: Standard Postoperative Care
Patients received standard postoperative care without a structured exercise program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative Neck Pain
Time Frame: Postoperative day 1 and postoperative day 10
|
Postoperative neck pain was assessed using the Visual Analog Scale (VAS), where scores range from 0 (no pain) to 10 (worst imaginable pain).
Assessments were performed on postoperative day 1 before discharge and on postoperative day 10 during follow-up by a blinded outcome assessor.
|
Postoperative day 1 and postoperative day 10
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck Discomfort and Early-Stage Quality of Life
Time Frame: Postoperative day 1 and postoperative day 10
|
Neck discomfort and early-stage quality of life were evaluated using the Neck Pain, Discomfort, and Early-Stage Quality of Life Questionnaire (NPDEPQ).
Assessments were conducted on postoperative day 1 and postoperative day 10 by a blinded outcome assessor.
|
Postoperative day 1 and postoperative day 10
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mertcan Ak, MD, Istanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, Department of General Surgery
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 8, 2024
Primary Completion (Actual)
April 30, 2025
Study Completion (Actual)
April 30, 2025
Study Registration Dates
First Submitted
February 3, 2026
First Submitted That Met QC Criteria
February 15, 2026
First Posted (Actual)
February 17, 2026
Study Record Updates
Last Update Posted (Actual)
February 17, 2026
Last Update Submitted That Met QC Criteria
February 15, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Cerrahpaşa Faculty of Medicine
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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