- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02468817
PTH And Calcium Responses to Exercise (PACE) in Older Adults
12. mars 2018 oppdatert av: University of Colorado, Denver
Exercise that causes a decline in serum Calcium (Ca) as a result of dermal Ca loss stimulates bone resorption via an increase in Parathyroid Hormone (PTH).
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Determine whether the magnitude of dermal Ca loss (i.e., sweating) during exercise is a determinant of the decline in iCa and increases in PTH and carboxy-terminal collagen crosslinks (CTX; marker of bone resorption).
The proposed experiment will address this by manipulating the rate of dermal Ca loss (moderate vs high sweating rate) to determine whether this is the trigger for the cascade described in Figure 1.
This will be achieved by having participants perform two identical exercise bouts under different thermal conditions (warm vs cool).
Studietype
Intervensjonell
Registrering (Faktiske)
12
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Colorado
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Aurora, Colorado, Forente stater, 80045
- University of Colorado Hospital
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-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
60 år til 80 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Healthy adults aged 60-80 y
Exclusion Criteria:
- Use of medications in the past 6 months known to affect bone metabolism (e.g., bisphosphonates, thiazide diuretics, oral glucocorticoids)
- BMD t score < -2.5 at the total hip or lumbar spine
- Known disease or condition associated with intestinal malabsorption
- Moderate or severe renal impairment defined as an estimated glomerular filtration rate of <60 mL/min/1.73m2 based on the MDRD equation
- Chronic hepatobiliary disease, defined as liver function tests (AST, ALT) >1.5 times the upper limit of normal; if such values are obtained on initial screening and thought to be transient in nature, repeated testing will be allowed
- Thyroid dysfunction, defined as an ultrasensitive TSH <0.5 or >5.0 mU/L; volunteers with abnormal TSH values will be re-considered for participation in the study after follow-up evaluation by the PCP with initiation or adjustment of thyroid hormone replacement
- Serum calcium <8.5 or >10.3 mg/dL
- Serum 25(OH)D <20 ng/mL; volunteers with abnormal serum 25(OH)D values may be re-considered for participation in the study if serum 25(OH)D is >20 ng/mL after vitamin D supplementation
- Uncontrolled hypertension defined as resting systolic BP >150 mmHg or diastolic BP>90 mmHg; participants who do not meet these criteria at first screening will be re-evaluated, including after follow-up evaluation by the PCP with initiation or adjustment of anti-hypertensive medications
- History of type 1 or type 2 diabetes
- Cardiovascular disease; subjective or objective indicators of ischemic heart disease (e.g., angina, ST segment depression) or serious arrhythmias at rest or during the graded exercise test (GXT) without follow-up evaluation will be cause for exclusion; follow-up evaluation must include diagnostic testing (e.g., stress echocardiogram or thallium stress test) with interpretation by a cardiologist
- Diagnosis or history of asthma
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Aktiv komparator: Treadmill Exercise
2 (two) 1-hour of vigorous exercise bouts under different thermal conditions, one at 16 degrees C and one at 26 degrees C.
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2 (two) 1-hour of vigorous exercise bouts under different thermal conditions
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Eksperimentell: Magnitude of Ca loss during Exercise at 26 degrees Celcius
Blood samples at 15-min intervals starting 15 min before exercise and ending 60 min after exercise.
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Blood samples at 15-min intervals starting 15 min before exercise and ending 60 min after exercise
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Parathyroid Hormone (PTH)
Tidsramme: 60 minutes of exercise and 2 hours of recovery
|
PTH will be measured during baseline, throughout exercise, and during recovery at regular intervals.
We are looking to see how PTH changes over the course of the exercise and recovery period in both the warm and cool conditions.
We anticipate that PTH will be higher in the warm condition versus the cool.
We expect that men and women will respond similarly.
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60 minutes of exercise and 2 hours of recovery
|
|
Change C-Telopeptide (CTX)
Tidsramme: 60 minutes of exercise and 2 hours of recovery
|
CTX will be measured during baseline, throughout exercise, and during recovery at regular intervals.
We are looking to see how PTH changes over the course of the exercise and recovery period in both the warm and cool conditions.
We anticipate that CTX will be higher during exercise and recovery in the warm condition versus the cool.
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60 minutes of exercise and 2 hours of recovery
|
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Change in Serum Ionized Calcium (iCa)
Tidsramme: 60 minutes of exercise
|
iCa will be measured during baseline, throughout exercise, and during recovery at regular intervals.
We are looking to see how PTH changes over the course of the exercise and recovery period in both the warm and cool conditions.
We expect that serum iCa will be higher in the cool condition versus the warm.
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60 minutes of exercise
|
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Change in Total Ca
Tidsramme: 60 minutes of exercise
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Total Ca will be measured during baseline, throughout exercise, and during recovery at regular intervals.
We are looking to see how PTH changes over the course of the exercise and recovery period in both the warm and cool conditions.
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60 minutes of exercise
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Sarah J Wherry, PhD, University of Colorado, Denver
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. august 2015
Primær fullføring (Faktiske)
1. juni 2017
Studiet fullført (Faktiske)
1. januar 2018
Datoer for studieregistrering
Først innsendt
2. juni 2015
Først innsendt som oppfylte QC-kriteriene
8. juni 2015
Først lagt ut (Anslag)
11. juni 2015
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
14. mars 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
12. mars 2018
Sist bekreftet
1. mars 2018
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 15-0250
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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