NCT07492290Not yet recruiting
Empirical Study on Lifestyle Intervention for Elderly Hypertensive Patients in Community Based on TTM Theory
Source: ClinicalTrials.gov · Last updated 25 Mar 2026
Brief summary (registry, in English)
This study intervention is based on TTM theory and implements lifestyle interventions, including nutritious diet, regular exercise, social support, sleep optimization, avoidance of addictive substances, and stress management. Through various means such as training, guidance, and motivation, motivation is formed, goals are determined, and habits are strengthened, ultimately leading to the development of a healthy lifestyle, control of blood pressure indicators, and improvement of quality of life and cognitive function. The intervention period is a total of 3 weeks, on line.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 106 (estimated)
- First submitted
- 4 Dec 2025
- Start date
- 1 Apr 2026
- Primary completion date
- 30 Sept 2026
- Lead sponsor
- Qu Shen
- Diseases
- High blood pressure
- NCT number
- NCT07492290
What you commit to
- Study type: Interventional
- Planned participants: 106
- From 1 Apr 2026 to the primary completion date, 30 Sept 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who currently have or have previously had mental disorders;
Other illness
- Exclude those with a history of severe heart, brain, kidney diseases or cancer;
Other
- Patients who are currently participating in other research projects.
Who the study is looking for
- Patients whose blood pressure measurements taken at community hospitals meet the hypertension criteria outlined in the Chinese Guidelines for the Prevention and Treatment of Hypertension (2024 revision);
- Aged 60-75 years old;
- Have certain abilities in reading, comprehension, and communication;
- Able to use a smartphone;
- In the pre-conscious/conscious/preparatory stage.
- Volunteer to participate in this study and sign the informed consent form.
Age in the registry: 60 years to 75 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.