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Active, Not Recruiting

NCT Number: NCT06058598

Exercise Training in Patients With Glaucoma

HIT GLAUCOMA is a multicenter exercise study for glaucoma patients between three institutes: the Department of Sport, Exercise and Health (DSBG) of the University of Basel, the Eye Clinic at the University Hospital Basel and the UZ Leuven (Belgium). The main objective of the study is to investigate the possibility of using exercise therapy to treat glaucoma. Participants will be randomly divided into two groups: Intervention and Control group. The intervention group will receive a high-intensity interval training plan, and the control group will receive lifestyle counseling and standard therapy. With this method, the study aims to validate an exercise therapy concept that could significantly improve disease progression and quality of life in patients with glaucoma.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Basel, Department of Sport, Exercise & Health

Basel, 4052, Switzerland

About this study

Approximately 57.5 million people are affected by primary open-angle glaucoma, and it is estimated that this number will increase to 111.8 million by 2040. Despite the high prevalence and critical outlook of the disease, the pathogenesis of glaucoma is still not fully understood and treatment options remain inadequate. In particular, for glaucoma with normal intraocular pressure, there is as yet no evidence-based effective treatment option. This particular type of glaucoma may, in part, be the result of impaired microvascular endothelial function. Physical training has a proven effect on vascular health; because glaucoma involves a vascular component, positive effects of high-intensity interval training can be assumed. Thus, it could be an effective treatment for glaucoma disease.

Patients will be randomly assigned to either the intervention or control group. Patients assigned to the intervention group will participate in a 6-month exercise training program followed by a 6-months non-supervised and home-based physical activity maintenance program. During the first 6 months, patients in the intervention group participate in 18 supervised exercise sessions at the DSBG, interspersed by unsupervised exercise interventions at home.

All patients will be seen at baseline, after three months and six months of aerobic exercise training, and after another six months of physical activity and exercise self-maintenance (intervention group) or control condition. Each subject will be asked to undergo standard ophthalmic examination, non-invasive retinal assessments, peripheral blood withdrawal, and additional peripheral vascular examinations. The study design is based on regular glaucoma follow-up intervals (every 6 months) and does not intervene with clinical care and governmental reimbursement of standard care. Patients will finish their study participation after 6 months of exercise training followed by 6 months of physical activity and exercise self-maintenance or control condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Voluntary written informed consent of the participant has been obtained prior to any screening procedures
  • Patients with primary open angle glaucoma (POAG), high tension glaucoma (HTG) and normal tension glaucoma (NTG), aged 40 - 75 years
  • In regular follow-up in either of the two study centres

Exclusion criteria

  • Patients having had glaucoma surgery within 6 months before start of the project
  • Patients with changes in topical medication or laser trabeculoplasty within 3 months before start of the project
  • Patients with very severe glaucoma (visual field mean deviation lower than -12Db)
  • Significant opacification of ocular media
  • Patients with life-threatening arrhythmia, signs of ischemia during CPET which preclude participation in an exercise trial
  • Patients with insulin treated diabetes, chronic obstructive pulmonary disease or cancer.
  • Patients doing ≥1 structured exercise training session per week or >150min of exercise/week assessed via the following two questions: a. On average, how many days per week do you engage in moderate to vigorous physical activity (like brisk walking)? b. On average, how many minutes per day do you engage in physical activity at this level? Calculate the total weekly minutes of exercise by multiplying a times b.
  • Mental or physical limitation precluding participation in a high intensity exercise program

Treatment and study plan

Exercise training

Other

6-months supervised exercise training + 6 months unsupervised exercise training

Lifestyle Counselling

Other

12-months of lifestyle counselling

Primary outcomes

  1. Microvascular health: retinal arteriolar and venular dilation and diameters

    Time frame: 6-months

    Retinal arteriolar and venular flicker light-induced dilation after six months; Retinal arteriolar and venular diameters after six months

Sponsors and collaborators

Lead sponsor

Henner Hanssen

Other

Collaborators

  • Universitaire Ziekenhuizen KU Leuven
  • University Hospital, Basel, Switzerland

Registry information

Official study title

High Intensity Interval Training in Patients With Glaucoma

Acronym: HIT GLAUCOMA

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Sep 28, 2023
Registry last updated
Dec 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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