Anderson-Fabry Disease Fitness Improvement Training (A-FAD-FIT)
Anderson-Fabry Sygdom Fitness Forbedring Træning: A-FAD-FIT
This study will evaluate physical function, cardiorespiratory fitness, muscle strength, and quality of life in patients with Fabry disease and assess the effects of a 12-week physiotherapy-led exercise programme. Participants will be non-randomly assigned to an exercise intervention group or a control group receiving no study-specific exercise intervention. The intervention group will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline. The control group will be assessed at baseline and 12 months after baseline.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Fabry disease is a rare X-linked lysosomal storage disorder associated with multisystem involvement, reduced exercise tolerance, fatigue, pain, and impaired quality of life. Evidence regarding structured physiotherapy and exercise interventions in this population remains limited.
The aim of this study is to evaluate functional and cardiorespiratory capacity in patients with Fabry disease and to investigate the effects of a 12-week physiotherapy-led exercise programme. Participants will be non-randomly assigned to either an exercise intervention group or a control group receiving no study-specific exercise intervention. Group assignment will primarily reflect participants' willingness to participate in the exercise programme and logistical feasibility, particularly the ability to attend regular supervised exercise sessions.
Participants in the intervention group will complete a 12-week physiotherapy-led programme consisting of one supervised exercise session per week and two home-based exercise sessions per week. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. The programme also includes a progressive increase in daily ambulatory physical activity, monitored primarily by daily step count. Participants in the intervention group will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline.
Participants in the control group will receive no study-specific exercise intervention and will be assessed at baseline and 12 months after baseline. The study will evaluate short-term changes following the exercise intervention as well as longer-term changes in the main study outcomes.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Jan Vávra, Masters
- Telefonnummer: +420601200272
- E-mail: Jan.Vavra2@vfn.cz
Studiesteder
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Prague, Tjekkiet, 12808
- Rekruttering
- General University Hospital
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Kontakt:
- Jan Vávra, Masters
- Telefonnummer: +420601200272
- E-mail: vavrajan1@gmail.com
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Kontakt:
- Vladimír Tuka, doc
- E-mail: Vladimir.Tuka@vfn.cz
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Confirmed diagnosis of Fabry disease
- Age 18 years or older
- Followed at a participating clinical center
- Able to understand the study procedures and provide informed consent
- Clinically stable and medically suitable for exercise testing and participation in the exercise programme
Exclusion Criteria:
- Acute deterioration in health status at the time of enrollment
- Medical contraindication to exercise testing or exercise training
- Severe comorbidity preventing safe participation in the study procedures
- Inability to comply with study procedures or complete follow-up assessments
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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Eksperimentel: Exercise Intervention Group
Participants will complete a 12-week physiotherapy-led exercise programme consisting of one supervised exercise session per week and two home-based exercise sessions per week, together with a progressive increase in daily step count. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. Participants will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline. |
A 12-week physiotherapy-led exercise programme consisting of one supervised session and two home-based exercise sessions per week. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. The programme also includes a progressive increase in daily ambulatory physical activity, monitored primarily by daily step count. Adherence is monitored using exercise diaries and regular follow-up during supervised sessions. |
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Ingen indgriben: Control Group
Participants will receive no study-specific exercise intervention. They will be assessed at baseline and 12 months after baseline. |
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change from baseline in peak oxygen uptake (VO2peak) after 12 weeks
Tidsramme: Baseline and 12 weeks after baseline
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Change from baseline in peak oxygen uptake (VO2peak), expressed in mL/kg/min, assessed during cardiopulmonary exercise testing (CPET) in the exercise intervention group following the 12-week exercise programme. |
Baseline and 12 weeks after baseline
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change from baseline in peak oxygen uptake (VO2peak) at 12 months
Tidsramme: Baseline and 12 months after baseline
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Change from baseline in peak oxygen uptake (VO2peak), expressed in mL/kg/min, assessed during cardiopulmonary exercise testing (CPET). VO2peak will be assessed at baseline and 12 months after baseline in both the exercise intervention and control groups. The change over 12 months will be compared between groups. |
Baseline and 12 months after baseline
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Change in handgrip strength
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in handgrip strength, expressed in kilograms, assessed using handgrip dynamometry. Participants will be assessed in a seated position with the arm close to the body and the elbow flexed at approximately 90 degrees. Three maximal trials will be performed for each hand. The highest value from each hand will be retained, and the mean of the highest right- and left-hand values will be used as the handgrip strength outcome. In the intervention group, handgrip strength will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, handgrip strength will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in 6-minute walk distance
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in distance walked during the 6-minute walk test, expressed in meters. In the intervention group, the 6-minute walk distance will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the 6-minute walk distance will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in 30-second chair stand test performance
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in the number of completed stands during the 30-second chair stand test. In the intervention group, performance will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, performance will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in forced expiratory volume in 1 second (FEV1)
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in forced expiratory volume in 1 second (FEV1), expressed in liters, assessed by pulmonary function testing. In the intervention group, FEV1 will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, FEV1 will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in vital capacity (VC)
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in vital capacity (VC), expressed in liters, assessed by pulmonary function testing. In the intervention group, VC will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, VC will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in diffusing capacity of the lungs for carbon monoxide (DLCO)
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in diffusing capacity of the lungs for carbon monoxide (DLCO), expressed in mmol/min/kPa, assessed by pulmonary function testing. In the intervention group, DLCO will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, DLCO will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in Hospital Anxiety and Depression Scale - Anxiety subscale score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in anxiety symptoms assessed using the Anxiety subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, resulting in a total score ranging from 0 to 21. Higher scores indicate greater severity of anxiety symptoms. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in Hospital Anxiety and Depression Scale - Depression subscale score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in depressive symptoms assessed using the Depression subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, resulting in a total score ranging from 0 to 21. Higher scores indicate greater severity of depressive symptoms. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Physical Functioning domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in physical functioning assessed using the Physical Functioning domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 10 items and is scored from 0 to 100, with higher scores indicating better physical functioning. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Role Physical domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in limitations in usual role activities due to physical health problems assessed using the Role Physical domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 4 items and is scored from 0 to 100, with higher scores indicating fewer limitations due to physical health problems. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Bodily Pain domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in bodily pain assessed using the Bodily Pain domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 2 items and is scored from 0 to 100, with higher scores indicating less pain and less interference of pain with usual activities. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 General Health domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in general health perceptions assessed using the General Health domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 5 items and is scored from 0 to 100, with higher scores indicating better perceived general health. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Vitality domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in vitality assessed using the Vitality domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 4 items and is scored from 0 to 100, with higher scores indicating greater vitality and lower levels of fatigue. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Social Functioning domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in social functioning assessed using the Social Functioning domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 2 items and is scored from 0 to 100, with higher scores indicating better social functioning and less interference of health problems with social activities. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Role Emotional domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in limitations in usual role activities due to emotional problems assessed using the Role Emotional domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 3 items and is scored from 0 to 100, with higher scores indicating fewer role limitations due to emotional problems. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in SF-36 Mental Health domain score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in mental health assessed using the Mental Health domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 5 items and is scored from 0 to 100, with higher scores indicating better mental health and psychological well-being. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in EQ-5D-5L health state index value
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in health-related quality of life assessed using the EQ-5D-5L descriptive system. The instrument assesses five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each rated across five levels of severity. Responses will be converted to an EQ-5D-5L health state index value using an appropriate validated value set. Higher index values indicate better health-related quality of life. In the intervention group, the index value will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the index value will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in EQ-5D-5L Visual Analogue Scale score
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in self-rated health assessed using the EQ-5D-5L Visual Analogue Scale (EQ VAS). The scale ranges from 0 to 100, where 0 represents the worst health the participant can imagine and 100 represents the best health the participant can imagine. Higher scores indicate better self-rated health. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in skeletal muscle mass
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in skeletal muscle mass, expressed in kilograms, assessed by bioelectrical impedance analysis using the InBody970 device. In the intervention group, skeletal muscle mass will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, skeletal muscle mass will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in body fat mass
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in body fat mass, expressed in kilograms, assessed by bioelectrical impedance analysis using the InBody970 device. In the intervention group, body fat mass will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, body fat mass will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in whole-body phase angle
Tidsramme: Baseline, 12 weeks after baseline, and 12 months after baseline
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Change in whole-body phase angle, expressed in degrees, assessed at 50 kHz by bioelectrical impedance analysis using the InBody970 device. In the intervention group, whole-body phase angle will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, whole-body phase angle will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Cerebrovaskulære lidelser
- Hjernesygdomme
- Sygdomme i centralnervesystemet
- Sygdomme i nervesystemet
- Karsygdomme
- Hjerte-kar-sygdomme
- Metabolisme, medfødte fejl
- Genetiske sygdomme, medfødte
- Metaboliske sygdomme
- Lipidmetabolismeforstyrrelser
- Genetiske sygdomme, X-forbundet
- Lysosomale opbevaringssygdomme
- Hjernesygdomme, metaboliske, medfødte
- Hjernesygdomme, metaboliske
- Lipidmetabolisme, medfødte fejl
- Lysosomale opbevaringssygdomme, nervesystemet
- Cerebrale småkarsygdomme
- Sphingolipidoser
- Lipidoser
- Medfødte, arvelige og neonatale sygdomme og abnormiteter
- Opførsel
- Ernæringsmæssige og metaboliske sygdomme
- Fabrys sygdom
- Motorisk aktivitet
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- A-FAD-FIT
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
There is currently no plan to share individual participant data. Any future data sharing would require separate consideration in accordance with applicable ethics, participant consent, and data protection requirements.
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