NCT07182578

Brief Summary

The goal of this pilot study is to create, implement, and evaluate an aquatic therapy for Postural Orthostatic Tachycardia Syndrome (POTS) program feasibility and ability to improve quality of life as determined by reduced orthostatic tachycardia, reduced POTS symptoms, and improved quality of life measures. The main questions it aims to answer are: Does aquatic occupational therapy reduce orthostatic tachycardia and POTS symptoms? Does aquatic occupational therapy lead to higher quality of live measures for people with POTS? Is this aquatic occupational therapy program feasible for clinicians and people with POTS? There is no comparison group for this pilot study. Participants will complete: An occupational Therapy evaluation before and after program completion (3 hours total) 30 minutes at home/remote 30 minutes on-site/in-person 30 minutes of individualized occupational therapy on land Participate in 3 aquatic therapy sessions per week, 60 minutes each for 12 weeks

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 10, 2025

Completed
2 days until next milestone

Study Start

First participant enrolled

September 12, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 19, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2026

Completed
Last Updated

September 19, 2025

Status Verified

September 1, 2025

Enrollment Period

5 months

First QC Date

September 10, 2025

Last Update Submit

September 16, 2025

Conditions

Keywords

Aquatic TherapyOccupational therapyPOTSPostural Orthostatic Tachycardia SyndromeDysautonomiaRehabilitationHydrotherapy

Outcome Measures

Primary Outcomes (9)

  • World Health Organization Quality of Life - Brief (WHOQOL-BREF)

    The WHOQOL-BREF is a 26-item questionnaire that will be completed digitally. It is scored by first assigning numerical values (1-5) to each response, with higher scores generally indicating a better quality of life. Then, raw domain scores are calculated by averaging the responses within each domain (Physical, Psychological, Social, and Environmental). Finally, these raw domain scores are transformed into scaled scores ranging from 0 to 100 by multiplying by 4. Higher scores on the 0-100 scale indicate a higher quality of life. The measure will be reported as a quality of life score.

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention

  • The DePaul Symptom Questionnaire (Short Form) (DSQ-SF)

    14-item-questionnaire which measures post-exertional malaise symptoms over the last 6 months. Each question requires two ratings, one for frequency (0 = none of the time and 4 = all of the time) and one for severity (0 = symptom not present and 4 = very severe). A frequency of at least 2 and a severity of at least 2 on any one of the 5 questions on the DSQ-SF subscale indicate that post exertional malaise is present. For each symptom, the frequency and severity scores are averaged, and then multiplied by 25 to create a composite score out of 100. The measure will be reported as a post exertional malaise score.

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention.

  • Composite Autonomic Symptom Score-31

    Measures neurodegenerative system symptoms through 31 patient-reported questions. Assessment is through six weighted domains: orthostatic intolerance \[10 points\]; vasomotor \[6 points\]; secretomotor \[7 points\]; gastrointestinal \[28 points\]; bladder \[9 points\] and pupillomotor \[15 points\]. A higher score indicates worse autonomic dysfunction. Simple yes or no questions are scored as 0 points for no and 1 point for yes. Questions about a specific site of symptoms or symptoms under specific circumstances are scored as 0 if not present and as 1 if present for each site or circumstance. All questions regarding the frequency of symptoms were scored as 0 points for rarely or never, 1 point for occasionally or sometimes, 2 points for frequently or "a lot of the time," and 3 points for almost always or constantly. All questions regarding the severity of symptoms were scored as 1 point for mild, 2 points for moderate, and 3 points for severe. The measure will be reported as a COMPASS score

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention.

  • Malmo POTS Scale (MAPS)

    This 12-item questionnaire assesses the specific POTS symptom burden over the past 3 months. Each question uses a visual analog scale from 0-10, with a maximum score of 120. A score of 42 or higher is considered indicative of POTS. The measure will be reported as a MAPS score.

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention

  • ADLS, IADLS, and Vestibular Questionnaire

    This is a 26-item questionnaire that will be filled out digitally. 21 questions cover about to participate in occupations listed in the Occupational Therapy Practice Framework using a scale from 1-10, where 1 is unable to complete the task, 5 is able to complete task with moderate difficulty (noticeable symptoms and extra effort is required) 10 is no problems/symptoms completing the task. It also contains 5 vestibular related questions using a scale from 1-7, with 1 being not at all dizzy, 4 being moderately dizzy, and 7 being extremely dizzy. The measure will be reported as an AIVQ score.

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention

  • Active Stand Test

    The patient will begin laying down in a relaxed and comfortable position. Blood pressure (BP) and heart rate (HR) are taken after 5 minutes. Next, the patient will be asked to stand promptly, and will have their BP and HR measured immediately. The therapist will note any comments like "feeling dizzy". The BP and HR will be taken again and documented after three minutes, and again after ten minutes of standing. If there is any event, such as severe dizziness, paleness, etc, the BP and HR will be taken and documented just before the patient sits down. The measure will be reported as the position, time, and the correlated heart rate and blood pressure.

    From enrollment until the end of treatment at 12 weeks

  • Single leg stance test

    This test measures a person's ability to balance standing on one leg without assistance. The participant will stand on one leg with their hands on their hips while being timed. The test is repeated 3 times for each leg and averaged. The measure will be reported as time standing per leg.

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention

  • Heart Rate

    Heart rate (HR) will be measured on land while the participant is laying down, sitting up, and standing. HR in the water will be taken while seated and standing. An aquatic HR maximum and HR zones will be calculated for each participant. This measure will be reported as a land-based and aquatic HR maximum.

    From enrollment to the end of treatment at 12 weeks

  • Borg's rate of perceived exertion scale

    This scale is used to tell how tiring an activity feels. The scale ranges from 6 (no exertion at all), to 20 (maximal heaviness). This will be reported as the RPE score.

    From enrollment to the end of treatment at 12 weeks

Secondary Outcomes (9)

  • The Stroop Test

    From enrollment to the end of 12 weeks of aquatic occupational therapy intervention

  • Trail Making Test Parts A & B

    From enrollment to the end of the intervention at 12 weeks

  • Enrollment

    From enrollment to the end of treatment at 12 weeks

  • Attrition Rate

    From enrollment to the end of treatment at 12 weeks

  • Session attendance rate

    From enrollment to the end of treatment at 12 weeks

  • +4 more secondary outcomes

Study Arms (1)

Aquatic Occupational Therapy Intervention

EXPERIMENTAL

All participants will participate in the aquatic occupational therapy arm. The aquatic occupational therapy intervention is divided into three progressive months: Month 1: Breathing techniques, proprioception, balance, and vestibular activities. Easy breathing and balancing moves Example: Belly breathing, water walking, toe lifts, mountain aqua yoga pose Month 2: Strength and endurance training Building strength and ability to exercise longer Example: Water marching, core exercises using dumbbells or paddles Month 3: Advanced strengthening and endurance tasks with integrated cognitive, balance, and dual-task challenges. Harder exercises and doing two things at once, like thinking and moving together Example: Dumbbell exercises while playing a word association game

Other: Aquatic Occupational Therapy

Interventions

Aquatic Occupational Therapy sessions will be 60 minutes long, with 45 minutes spent in the pool. Sessions will include a gentle floating, stretching, or aqua yoga warm-up and an ai chi cooldown. Exercises in the first month will include a focus on balance, breathing, and sensory work. Exercises in the second month will focus on building strength and endurance, while the third month will combine all of the above with dual-task completion. Activities will be graded down (made less difficult) or graded up (made more challenging) according to individual participant needs.

Aquatic Occupational Therapy Intervention

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosed with POTS, Age 18-64, Participants must be English speaking, participants must obtain a physician permission letter\* \* The physician letter will only state that the participant is cleared to participate in aquatic therapy, it will not confirm or state what disease the individual has in the medical records or other HIPAA information.

You may not qualify if:

  • Not diagnosed with POTS, Not between the ages of 18-64\*, Epilepsym Bowel incontinence
  • \*The reason for the age requirement is because individuals:
  • under 18 have different diagnostic criteria and mechanisms for POTS than the age range specified and may respond differently to treatment
  • over age 65 have different mechanisms behind POTS than younger individuals, and frequently have health conditions or factors that can be difficult to differentiate from POTS symptoms/diagnosis and would require lab work and continuous physician involvement. POTS is less common in older adults.
  • The typical age of onset for POTS is generally considered to be between the ages of 15-50 years of age
  • For participant's safety, the researcher needs to be able to communicate with them in the aquatic setting. English is the researcher's only language and electronic translators are not accessible/usable in the pool setting.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

California Aquatic Therapy & Wellness Center

Long Beach, California, 90805, United States

RECRUITING

MeSH Terms

Conditions

Postural Orthostatic Tachycardia SyndromeAutonomic Nervous System Diseases

Condition Hierarchy (Ancestors)

Orthostatic IntolerancePrimary DysautonomiasNervous System Diseases

Study Officials

  • EvaRose Celeste, OT Doctoral student

    California State University, Dominguez Hills

    PRINCIPAL INVESTIGATOR
  • Tracy Becerra-Culqui, PhD, MPH, BS OT

    California State University, Dominguez Hills

    STUDY CHAIR

Central Study Contacts

EvaRose Celeste, OT Doctoral student

CONTACT

Tracy Becerra-Culqui, PhD, MPH, BS OT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investivator

Study Record Dates

First Submitted

September 10, 2025

First Posted

September 19, 2025

Study Start

September 12, 2025

Primary Completion

January 30, 2026

Study Completion

January 30, 2026

Last Updated

September 19, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

The final dataset will include individual-level vaccination and demographic data, as well as other health characteristics. We will make the data and associated documentation available to users only under a data-sharing agreement that provides for: (1) a commitment to using the data only for research purposes and not to identify any individual participant; (2) a commitment to securing the data using appropriate computer technology; and (3) a commitment to destroying or returning the data after analyses are completed. We will share the final dataset under our own auspices and by our own determination based on review of a detailed research plan submitted by the requestor.

Locations