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N/A Completed N=40 Randomized Single-blind Supportive Care

Breathwork App for Cancer Survivors

Source: ClinicalTrials.gov NCT05161260 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcomePrimary: Total Practice Time as Assessed in Minutes Within the Study Application. — 0.2; 0.2 Minutes

Summary

Cancer survivorship is associated with many long-term chronic health issues that arise as a result of cancer treatment protocols. Non-pharmacological lifestyle and mind-body interventions have been shown to be effective and critical components of a total-health strategy for cancer survivors. PranaScience Institute seeks to develop and test a novel group video app for home-based delivery of a Yogic Breathing intervention that reduces symptoms of cancer treatment survival and supports total-health.

Outcome Measures

OutcomeResultp-value
PRIMARY
Total Practice Time as Assessed in Minutes Within the Study Application.
0.2; 0.2
PRIMARY
Practice Frequency as a Measure of Adherence
20; 60
PRIMARY
Participants' Symptom Management as Measured by the System Usability Scale.
60; 20
SECONDARY
Change in Perceived Stress (Perceived Stress Scale-10)
-1.54; -3.65
SECONDARY
Change in Depression Symptoms (Depression Scale)
-3.55; -0.29
SECONDARY
Change in Symptom Burden (MD Anderson Symptom Inventory)
-5.96; -3.68

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older, willing to provide informed consent.
  • Diagnosis of Stage 0-III breast cancer.
  • Completion of radiation therapy within the last 6 months.
  • ECOG performance status of 0-3 during cancer treatment.
  • Orally expressed visual and auditory acuity adequate for filling out all study forms and participating in telephone interviews and internet-based group video applications.
  • Access to telephone and internet-connected computer or mobile phone.

Exclusion Criteria

  • Subject is unwilling or unable to comply with any of the study procedures.
  • Orally expressed dependence on alcohol or drugs.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05161260). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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