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A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen for HYpothyroidism' (Q'SHY)

A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen for HYpothyroidism' (Q'SHY)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04784208
Acronym
STRI
Enrollment
232
Registered
2021-03-05
Start date
2021-01-18
Completion date
2022-12-31
Last updated
2022-07-13

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

Conditions

Healthy, Hypothyroidism

Brief summary

Type of Study Questionnaire- Development and validation Information about the Q'SHY: * The Q'SHY- Questionnaire for Screening of Hypothyroidism is a Patient Reported Outcome (PRO) tool to enable screening for Hypothyroidism in the general population. * It is a 20-item questionnaire which covers aspects of the symptoms of Hypothyroidism and incorporates the contributory factors from patient history which when combined, provides a robust tool to effectively screen the population. * The questionnaire content is being created based on a thorough search for relevant literature and encompasses all important aspects for screening purposes

Detailed description

Objectives The objectives of the study are as described in the below points. 1. To develop a questionnaire (Q'SHY) for the identification and screening of subjects with suspected hypothyroidism. 2. To assess the validity of the designed questionnaire by comparing the outcomes of the responses between General population subjects and treatment naïve subjects group with hypothyroidism. 3. The study aims to establish a valid questionnaire with a robust sensitivity and specificity to detect signs and symptoms of hypothyroidism. Inclusion criteria for Subjects The criteria based on which, subjects in each Arm will be chosen to take part in the survey. Arm1: Subjects from the general population who are naïve to their hypothyroid status. * Male and female subjects between the age of 18 years and 65 years * Willing to sign the Subject Authorization Form (SAF) Arm 2: Subjects who are newly diagnosed patients of Hypothyroidism and are treatment naïve\*. * Male and female subjects between the ages 18 years and 65 years. * Subjects who had symptoms of hypothyroidism were seen by a physician and diagnosed with hypothyroidism after laboratory testing of Thyroid Stimulating Hormone \> 4.5 Milli international units per litre(mIU/L) within 2 weeks from the date of the survey * Willing to sign the SAF * Willing to provide their Thyroid Function Test report that was used to diagnose Hypothyroidism. \* Treatment naive diagnosed on basis lab and clinical diagnosis within last 2 weeks Exclusion criteria for subjects Arm 1: Subjects from the general population who are naïve to their hypothyroid status * Individuals less than 18 years of age and more than 65 years of age. * Pregnant or lactating females Subjects previously diagnosed with and received treatment for thyroid diseases. * Subjects not willing to sign the SAF. Arm 2: Subjects who are newly diagnosed patients of Hypothyroidism and are treatment naïve * Individuals less than 18 years of age and more than 65 years of age. * Pregnant or lactating females * Subjects previously diagnosed with and received treatment for thyroid diseases. * Patients on treatment for Thyroid diseases Subjects not willing to sign the SAF. The above-mentioned criteria will be applicable to both Face validation and Pilot survey. 1. Subjects are divided into 2 arms, with 100 subjects in each arm. 2. Phase -1 * Arm 1: Sixteen subjects from the general population who are naïve to their hypothyroid status with equal distribution of males and females. * Arm 2: Sixteen subjects who are newly diagnosed patients of Hypothyroidism are treatment naïve with equal distribution of males and females 3. Phase -2 * Arm 1: One hundred subjects from the general population who are naïve to their hypothyroid status with equal distribution of males and females * Arm 2: One hundred subjects who are newly diagnosed patients of Hypothyroidism are treatment naïve with equal distribution of males and females

Interventions

DIAGNOSTIC_TESTBlood test for Thyroid stimulating hormone (TSH)

Blood test for Thyroid stimulating hormone (TSH)

Sponsors

Abbott
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* The criteria based on which, subjects in each Arm will be chosen to take part in the survey. Arm 1: Subjects from the general population who are naïve to their hypothyroid status. * Male and female subjects between the age of 18 years and 65 years * Willing to sign the Subject Authorization Form (SAF) Arm 2: Subjects who are newly diagnosed patients of Hypothyroidism and are treatment naïve\*. * Male and female subjects between the ages 18 years and 65 years. * Subjects who had symptoms of hypothyroidism, were seen by a physician and diagnosed with hypothyroidism after laboratory testing of TSH \> 4.5 mIU/L within 2 weeks from the date of survey * Willing to sign the SAF * Willing to provide their Thyroid Function Test report that was used to diagnose Hypothyroidism. \* Treatment naive diagnosed on basis lab and clinical diagnosis within last 2 weeks

Exclusion criteria

* Arm 1: Subjects from the general population who are naïve to their hypothyroid status * Individuals less than 18 years of age and more than 65 years of age. * Pregnant or lactating females * Subjects previously diagnosed with and received treatment for thyroid diseases. * Subjects not willing to sign the SAF. Arm 2: Subjects who are newly diagnosed patients of Hypothyroidism and are treatment naïve * Individuals less than 18 years of age and more than 65 years of age. * Pregnant or lactating females * Subjects previously diagnosed with and received treatment for thyroid diseases. * Patients on treatment for Thyroid diseases Subjects not willing to sign the SAF. The above-mentioned criteria will be applicable to both Face validation and Pilot survey.

Design outcomes

Primary

MeasureTime frameDescription
To be able to develop a questionnaire (Q'SHY) for the identification and screening of subjects with suspected hypothyroidismthrough out the study upto 1 yearThe aim is to develop a questionnaire considering literature review for symptoms selection, medical review of symptoms appropriateness, assigning weightage & questionnaire construction followed by expert review to construct a questionnaire
To be able to assess the validity of the designed questionnaire by comparing the outcomes of the responses between General population subjects and treatment naïve subjects group with hypothyroidism.through out the study upto 1 yearThrough this study, we want to assess the validity of the questionnaire after receiving and comparing responses received from healthy volunteers and treatment naïve subjects with hypothyroidism through out the study we will have face validation of survey questionnaire - Face validation of survey questionnaire in hypothyroidism naïve and treatment naïve patients of hypothyroidism, revision of questionnaire if required after expert review of validation results
To be able to establish a valid questionnaire with a robust sensitivity and specificity to detect signs and symptoms of hypothyroidismthrough out the study upto 1 yearin this, Pilot survey in hypothyroidism naïve and treatment naïve patients of hypothyroidism will be conducted and data will be analyzed and used to establish validation.

Countries

India

Contacts

Primary ContactDr Prasanna Kumar
dr.kmpk@gmail.com919845156811

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026