All patients with hypothyroidism are currently treated the same way, regardless of age. The investigators want to look at whether people aged 80 years or older would benefit from being treated with lower doses of levothyroxine. There are three reasons why the investigators think this could be beneficial, but this is not yet proven: 1. Some older people with hypothyroidism may have few symptoms. 2. Doctors look at the amount of Thyroid Stimulating Hormone (TSH) in the patient's blood to decide the dose of Thyroxine received. The standard "normal" TSH range used to determine the dose of levothyroxine is from younger people. The investigators wonder whether this is appropriate to all age ranges particularly as the investigators know that older people may normally have higher TSH values. 3. If TSH levels are too low there may be a slight increased risk of problems such as brittle bones or an irregular heartbeat. The best way to test whether older people benefit from lower doses of levothyroxine is by a large clinical trial. Before the investigators can do this, the investigators need to run a smaller clinical trial called a "pilot study" (SORTED 1) to examine whether this is practical and acceptable. The pilot study aims to recruit 50 patients with hypothyroidism aged 80 or above. Participants will be randomly allocated to receive their routine or lower dose of levothyroxine. Follow-up will be conducted over approximately 25 weeks. The investigators also propose a qualitative study (SORTED 2) to specifically understand patient's willingness to take part in a RCT and participant's experience of the intervention. Finally, the investigators propose a retrospective cohort study of 400 treated hypothyroid patients aged 80 years or more registered in 2008 in Primary Care Practices with the aim of studying outcomes after 4 years. The cohort study will collect data required to inform a sample size calculation for a future full study where the primary outcome will be 4 year mortality.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
48
Participants in the lower dose arm of the study will receive a lower dose of levothyroxine than their usual dose
Participants in the standard dose of treatment will receive their usual dose of levothyroxine
Bensham Hospital
Gateshead, Tyne and Wear, United Kingdom
Clinical Research Facility
Newcastle upon Tyne, Tyne and Wear, United Kingdom
Participant's acceptability of study design and willingness to enter study
Participant's acceptability of study design as measured byt he completion rate of participants in each randomised group, as well as their willingness to enter the trial (consented participant to eligible participant approached ratio)
Time frame: Until completion of recruitment, approximately 24 months
Participant recruitment rate
As measured by the number of patients randomised divided by the length of the recruitment period. The recruitment period runs from the date that recruitment opened to the date of last randomisation.
Time frame: Until completion of recruitment, approximately 24 months
Time to achieve desired TSH levels
To review and assess the dose titration strategy (ie reduced LT4 dose or same dose LT4) and length of time required to achieved desired TSH levels (ie number of participants in each group that reach target TSH range at both 12 and 24 weeks)
Time frame: Until participant completion of SORTED 1 study, approximately within 24 weeks
Medication compliance
Tablet count
Time frame: For the duration of participant involvment in the study, maximum of 25 weeks
The acceptability of three patient completed questionnaires
The questionnaires include the generic QoL questionnaire (EQ-5D), validated disease-specific QoL questionanaire (ThyDQol) and disease specific hypothyroid-symptom check list (ThySC). The time taken to complete the three questionnaires will be recorded and questionnaire completion rates will be recorded and usefulnesss of questionnaires determined. Any third-party held required in a questionnaire's completion will be recorded.
Time frame: For the duration of participant involvement in the study, maximum of 25 weeks
Assessment of mobility
Measured by the nurse administered TUG Test, and the FRAT (Falls Risk Assessment Tool)
Time frame: For the duration of participant involvement in this study, maximum of 25 weeks
Change in specific cardiovascular risk factors
Lipid profile (total cholesterol, HDL, Triglycerides), blood pressure and body weight, and serum results
Time frame: For the duration of participant involvement in the study, maximum of 25 weeks
Measure of risk of falls
Measure by nurse administrated FRAT (Falls Risk Assessment Tool) test.
Time frame: For the duration of participant involvement in the study, maximum 25 weeks
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