Actively Recruiting
Individualized Physical Activity or Patients With Non Functioning Pituitary Adenoma
Led by Vastra Gotaland Region · Updated on 2025-09-17
120
Participants Needed
1
Research Sites
200 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn about physical activity's effect on health in people who have had surgery of a non-functioning pituitary adenoma. The main questions it aims to answer are: * Do physical activity increase quality of life? * Do physical activity increase general health, cardiovascular fitness, self-efficacy and muscle strength and reduce fatigue and cardiovascular risk profile? Participants will at the start of the the study, at 6 months follow up and 12 months follow up: * Fill out health surveys * Perform a cycling test, hand strength test, chair stand test and wear and accelerometer for a week * Undergo a dual energy X-ray absorptiometry to measure muscle and fat mass * Leave blood samples Researchers will compare those who are randomized to the intervention and see a physiotherapist to get an individualized and person-centred prescription of physical activity plan and those who are randomized not to be in the intervention to see if physical activity increases quality of life and general health.¨.
CONDITIONS
Official Title
Individualized Physical Activity or Patients With Non Functioning Pituitary Adenoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with clinically significant non-functioning pituitary adenoma treated with surgery during the last ten years
- Stable hormone replacement therapy for at least 6 months
- Ability to communicate in Swedish
- Age between 18 and 75 years
You will not qualify if you...
- Patients with any other pituitary tumors than non-functioning pituitary adenoma
- Patients who may need tumor intervention (surgery or radiotherapy) within one year
- Ongoing substance abuse or untreated psychiatric disorders except mild/moderate depression or anxiety treated with SSRI or SNRI
- Use of opioids, sedatives, or hypnotics except zopiclone and zolpidem
- History of neurological diseases with impaired mobility
- High alcohol consumption (more than 14 units per week)
- Ongoing cancer treatment
- Uncontrolled hypertension or significant cardiac disease
- Severe respiratory insufficiency
- Severely impaired liver function (ALT or AST two times above normal)
- Severely impaired kidney function (glomerular filtration rate below 45 ml/min)
- Untreated hypo- or hyperthyroidism
- Pregnancy or breastfeeding
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sahlgrenska Univesity Hospital
Gothenburg, Västra Götaland County, Sweden, 41345
Actively Recruiting
Research Team
V
Victor Hantelius, Md
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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