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Guildford HyperTension 2000: Exercise interventions to increase levels of physical and sporting activity

Guildford Hypertension 2000: randomised trial of exercise interventions to increase levels of physical and sporting activity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN71952900
Enrollment
2000
Registered
2013-06-14
Start date
2013-09-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

Currently inactive 18-74 year old people with hypertension, suspected hypertension, pre-hypertension or high-normal blood pressure. Circulatory System Hypertension

Interventions

1. The first intervention is a web-based behaviour change support tool, that allows users to easily find out about outlets for organised activity, form and store plans to carry out the activities and

Sponsors

University of Surrey (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient is aged 18 to 74 years at randomisation 2. The patient has been diagnosed as having hypertension, suspected hypertension and pre-hypertension 3. The patient is screened as being ?less than active? on the General Practice Physical Activity Questionnaire (GPPAQ) 4. The patient has access to the internet and an e-mail account 5. The patient is able to understand the Informed Consent Form (ICF), and understand study procedures 6. The patient has signed the ICF

Exclusion criteria

Exclusion criteria: 1. The patient is pregnant 2. Inability to freely consent to take part in the study 3. Inability to understand the study materials 4. The patient is unable to access the internet/email 5. Current participation in another clinical trial relating to physical activity or exercise 6. Any condition that, in the GP?s opinion, compromises the subject?s ability to meet protocol requirements or to complete the study 7. The patient is referred out of the trial by the exercise professional on the grounds that the programme is, in their judgement, is likely to cause harm

Design outcomes

Primary

MeasureTime frame
The interventions individually will be regarded as successful if they lead to an average increase in activity of 100 Metabolic Equivalents (MET) -minutes per week as measured by the IPAQ-S. This equates to engaging in an extra moderate intensity activity, say brisk walking (3.3 MET) for 30 minutes per week. The new interventions will be regarded as superior to the standard gym-based referral if they increase activity levels above those of the standard care gym-based exercise by 20 MET-minutes per week. Activity will be measured at baseline, 12 weeks, 6 months and 12 months.

Secondary

MeasureTime frame
1. We will assess changes in indicators relating to cardiovascular health including blood pressure, weight and waist and hip circumference at baseline, 6 weeks, 12 weeks and 12 month. In terms of blood pressure the interventions will be regarded as successful if they lead to an average decrease in blood pressure of 2.5mmHg. We will assess the proportion of the sample reducing their blood pressure by more than 10 mmHg and an intervention will be regarded as a success if more than 20% of the members of that study arm achieve a reduction greater than this. 2. The interventions will be deemed to have been successful in promoting sports participation if they increase sports related activity by 100 MET-minutes per week.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 19, 2026