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Not yet recruiting NCT07492290

Empirical Study on Lifestyle Intervention for Elderly Hypertensive Patients in Community Based on TTM Theory

No phase Interventional Hypertension (HTN) Age More 60yr

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Lifestyle medicine.
Who it may be relevant to
Registry conditions: Hypertension (HTN), Age More 60yr. Basic parameters: 60 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Interventions

  • Behavioral Lifestyle medicine
    Lifestyle medicine includes Nutrition , Physical Activity , Stress Management, Restorative Sleep , Social Connectedness, Avoidance of Risky Substances .

Primary outcome measures

  • blood pressure [Time frame: Baseline, the end of treatment at 3 weeks, and after 3 months]
  • Patient quality of life (SF-36) [Time frame: Baseline, the end of treatment at 3 weeks, and after 3 months]
Secondary outcome measures (2)
  • Patient cognitive function (AD8) [Time frame: Baseline, the end of treatment at 3 weeks, and after 3 months]
  • Patients' lifestyle (HPLP Ⅱ) [Time frame: Baseline, the end of treatment at 3 weeks, and after 3 months]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

  • Exclude those with a history of severe heart, brain, kidney diseases or cancer;
  • Patients who currently have or have previously had mental disorders;
  • Patients who are currently participating in other research projects.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07492290 · XDYX202509K38

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗