Individualized Physical Activity or Patients With Non Functioning Pituitary Adenoma

Non-functioning Pituitary Adenoma Clinical Trial

Official title:

Individualized and Person-centred Physical Activity and Exercise for Patients With Non Functioning Pituitary Adenoma - A Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06163261
• Other study ID #: PEPP
• Status: Recruiting
• Phase: N/A
• Start date: February 27, 2024
• Est. completion date: December 31, 2027

Study information

• Verified date: November 2023
• Source: Vastra Gotaland Region
• Contact: Victor Hantelius, Md
• Phone: +46704442085
• Email: victor.hantelius[@]vgregion.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.¨.

Description:

This study is an unblinded, prospective, randomized, controlled trial where 120 participants will be assigned to either an intervention group or a control group - 60 in each arm. The intervention will receive an individualized and person-centred prescription of physical activity and exercise. The control group will get standard care.

Inclusion criteria

• Patients with non-functioning pituitary adenoma treated with surgery the last ten years

• Stable hormone replacement therapy ≥ 6 months

• Age 18-75 years

• Ability to communicate in Swedish.

Exclusion criteria

• Patients with other pituitary tumours than non-functioning pituitary adenoma

• Patients who could need tumour intervention (surgery or radiotherapy), within one year

• Co-morbidities that could have significant impact on the outcome variables

After the randomization, patients in intervention arm will meet a physiotherapist and a research nurse. The participants will be asked to describe their life situation and experiences regarding their health, diseases, physical activity and exercise and after this be given an individualized and person-centred prescription of physical activity. The exercise will be documented in the self-care plan. In order to assess participants adherence to exercise, participants will be informed to document their performed exercise in the self-care plan during the first 12 weeks. All patients in the intervention group will be followed at 4, 8 and 12 weeks after inclusion in the study when they meet with the same nurse and physiotherapist as at the first visit.

Regarding outcome measures the primary endpoint and the secondary endpoints and will be measured at baseline, and at 6 and 12 months for both the intervention group and the standard care group. The primary endpoint is quality of life and the secondary endpoints are changes in health status, physical activity, cardiorespiratory fitness, muscle strength, self-reported fatigue and self-efficacy, and changes in cardiovascular risk profile.

To assess this the participant will:

• 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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: December 31, 2027
• Est. primary completion date: December 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients with clinically significant non-functioning pituitary adenoma treated with surgery during the last ten years

• Stable hormone replacement therapy = 6 months

• Ability to communicate in Swedish.

Exclusion Criteria:

• Patients with any other pituitary tumors than non-functioning pituitary adenoma

• Patients who possibly need tumor intervention, either with surgery or radiotherapy, within one year

• Other diseases or co-morbidities that may have significant impact on the outcome variables, including:

• Ongoing substance abuse and/or untreated psychiatric disorder, including psychoses and bipolar disease (except treatment with SSRI (Selective Serotonin Reuptake Inhibitor) and or SNRI (Serotonin-Norepinephrine Reuptake Inhibitor) for mild/moderate depression and/or anxiety which is allowed).

• Medical therapy with opioids, sedatives or hypnotics (besides treatment with zopiclone and zolpidem which are allowed).

• Current or previous history of neurological diseases with impaired mobility.

• High alcohol consumption (more than 14 alcohol units per week)

• Ongoing treatment for cancer.

• Uncontrolled hypertension or presence of clinically significant cardiac disease

• Severe respiratory insufficiency.

• Severely impaired hepatic function (ALT (Alanine Aminotransferase) and/or AST (Aspartate Aminotransferase) concentrations two times above the upper limit of normal).

• Severely impaired renal function (Glomerular filtration rate <45 ml/min).

• Untreated hypo- or hyperthyroidism

• Pregnancy or breast feeding.

Related Conditions & MeSH terms

• Adenoma
• Non-functioning Pituitary Adenoma
• Pituitary Diseases
• Pituitary Neoplasms

Intervention

Other:
• Physical activity
The intervention group will receive an individualized and person-centred prescription of physical activity and exercise.

Locations

Country	Name	City	State
Sweden	Sahlgrenska Univesity Hospital	Gothenburg	Vastra Gotaland

Sponsors (1)

Lead Sponsor	Collaborator
Vastra Gotaland Region

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in quality of life	Measured with the Short Form Survey Instrument (SF-36), where the score is transformed to a scale 0-100 where 100 represents be best possible health status and quality of life..	At baseline
Primary	Changes in quality of life	Measured with the Short Form Survey Instrument (SF-36), where the score is transformed to a scale 0-100 where 100 represents be best possible health status and quality of life..	At 6 months follow up
Primary	Changes in quality of life	Measured with the Short Form Survey Instrument (SF-36), where the score is transformed to a scale 0-100 where 100 represents be best possible health status and quality of life..	At 12 months follow up
Secondary	Changes in health status	Measured with EuroQol-5D (EQ5D). The EuroQol-5D (EQ-5D) index ranges from 0 to 1, where 1 represents the best possible health state, and a visual analog scale (VAS), a scale from 0 to 100, with 100 representing the best imaginable health state.	At baseline
Secondary	Changes in health status	Measured with EuroQol-5D (EQ5D). The EuroQol-5D (EQ-5D) index ranges from 0 to 1, where 1 represents the best possible health state, and a visual analog scale (VAS), a scale from 0 to 100, with 100 representing the best imaginable health state.	At 6 months follow up
Secondary	Changes in health status	Measured with EuroQol-5D (EQ5D). The EuroQol-5D (EQ-5D) index ranges from 0 to 1, where 1 represents the best possible health state, and a visual analog scale (VAS), a scale from 0 to 100, with 100 representing the best imaginable health state.	At 12 months follow up
Secondary	Changes in fitness/muscle strength - Cycling	Cycling test	At baseline
Secondary	Changes in fitness/muscle strength - Cycling	Cycling test	At 6 months follow-up
Secondary	Changes in fitness/muscle strength - Cycling	Cycling test	At 12 months follow up
Secondary	Changes in fitness/muscle strength - Hand strength	Hand strength test	At baseline
Secondary	Changes in fitness/muscle strength - Hand strength	Hand strength test	At 16 months follow up
Secondary	Changes in fitness/muscle strength - Hand strength	Hand strength test	At 12 months follow up
Secondary	Changes in fitness/muscle strength - Chair stand	Chair stand test	At baseline
Secondary	Changes in fitness/muscle strength - Chair stand	Chair stand test	At 6 months follow up
Secondary	Changes in fitness/muscle strength - Chair stand	Chair stand test	At 12 months follow up
Secondary	Changes in fitness/muscle strength - Accelerometer	Accelerometer for a week	At baseline
Secondary	Changes in fitness/muscle strength - Accelerometer	Accelerometer for a week	At 6 months follow up
Secondary	Changes in fitness/muscle strength - Accelerometer	Accelerometer for a week	At 12 months follow up
Secondary	Changes in self-reported self-efficacy	Self-reported self-efficacy through Self-Efficacy t Manage Chronic Disease (a questionnaire with 6 question where you rate yourself 1-10)	At baseline
Secondary	Changes in self-reported self-efficacy	Self-reported self-efficacy through Self-Efficacy t Manage Chronic Disease (a questionnaire with 6 question where you rate yourself 1-10)	At 6 months follow up
Secondary	Changes in self-reported self-efficacy	Self-reported self-efficacy through Self-Efficacy t Manage Chronic Disease (a questionnaire with 6 question where you rate yourself 1-10)	At 12 months follow up
Secondary	Changes in cardiovascular risk profile - Blood pressure	Blood pressure - systolic and diastolic	At baseline
Secondary	Changes in cardiovascular risk profile - Blood pressure	Blood pressure - systolic and diastolic	At 6 months follow up
Secondary	Changes in cardiovascular risk profile - Blood pressure	Blood pressure - systolic and diastolic	At 12 months follow up
Secondary	Changes in cardiovascular risk profile - Blood samples	Blood lipids	At baseline
Secondary	Changes in cardiovascular risk profile - Blood samples	Blood lipids	At 6 months follow up
Secondary	Changes in cardiovascular risk profile - Blood samples	Blood lipids	At 12 months follow up