Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People of any gender are eligible
- People who speak German or Italian
- People who have been diagnosed with a spine condition
- People aged 14 years or older
- People who consider themselves to be cognitively intact (thinking and memory functioning normally, based on their own assessment)
Who may not be able to join:
- People who are currently pregnant (based on self-reporting)
- People who are receiving medical or medication-based treatment for sleep disorders
- People who are taking melatonin
- People who use a smartwatch or app every day to automatically track their sleep
- People who are unable to give informed consent to participate in the trial
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 0443857148
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Translation and cross-cultural adaptation of the Single-item Sleep Quality Scale (SQS) in Italian and German; Field-testing of the Single-item Sleep Quality Scale (SQS) final translated version for responsiveness; Field-testing of the Single-item Sleep Quality Scale (SQS) final translated version for construct validity; Pilot-testing of the Single-item Sleep Quality Scale (SQS) pre-final translated version for content validity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.