Impact of Manual Therapy on Laryngeal Function Following Total Thyroidectomy
Launched by JOHNS HOPKINS UNIVERSITY · Apr 22, 2024
Trial Information
Current as of September 08, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how effective a combination of voice therapy techniques can be for people who experience changes in their voice or swallowing after having their thyroid gland completely removed (a procedure known as total thyroidectomy). The researchers want to find out if adding neck massage, stretching exercises, and education about pain can help improve these issues compared to just using voice exercises and scar massage alone. They hope to determine if these additional techniques can make a difference in how patients feel about their swallowing, voice, and overall quality of life after surgery.
To participate in the study, you need to be at least 18 years old and scheduled for a total thyroidectomy due to thyroid disease. You should be a native English speaker and have no previous voice therapy. Those who smoke or have certain voice or throat conditions may not be eligible. Participants will attend a total of four visits with their surgeon and five sessions with a speech therapist, where they'll practice exercises and keep a journal of their home practice. This trial is currently recruiting participants, so if you think this might apply to you, consider discussing it with your healthcare provider.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • The study population consists of individuals with malignant or benign thyroid disease scheduled to undergo total thyroidectomy
- • native speakers of English
- • All patients will be greater than or equal to 18 years of age
- Exclusion Criteria:
- • Participants will be excluded if they have completed voice therapy prior
- • are current smokers
- • have organic vocal fold pathology or clear mucosal changes to the vocal folds that can affect vibration (e.g., vocal fold scar, polyp, or nodules),
- • pre-existing unilateral or bilateral vocal fold paralysis
- • have had prior surgical neck or chest history including central or lateral neck dissection
- • pre- or post-operative abscess or inflammation
- • have a history of radiation, chronic cervical pain or cervicalgia, abnormal baseline swallowing
- • have underlying and, or plan to change supplemental hormones
- • greater than 10% otherwise unexplained weight loss
- • had a recent aspiration pneumonia
- • history of esophageal interventions or surgeries
About Johns Hopkins University
Johns Hopkins University, a prestigious research institution located in Baltimore, Maryland, is renowned for its commitment to advancing medical science and public health through innovative clinical trials. With a rich history of groundbreaking research and a multidisciplinary approach, the university's clinical trial initiatives focus on translating scientific discoveries into effective treatments and interventions. Leveraging state-of-the-art facilities and a collaborative network of experts, Johns Hopkins University conducts rigorous clinical studies that aim to improve patient outcomes and address critical health challenges. Its dedication to ethical standards and participant safety underscores its role as a leader in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Baltimore, Maryland, United States
Bethesda, Maryland, United States
Patients applied
Trial Officials
Vaninder Dhillon, MD
Principal Investigator
Johns Hopkins University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported