Clinical trial · Interventional
Tailored Home-Based Exercise Program for Multiple Chronic Conditions
Assessment of a Tailored Home-Based Exercise Program on Symptoms, Well-Being, and Resilience Among Cancer Survivors With Multiple Chronic Conditions
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A home-based, tailored, technology-enhanced home-based exercise program (iHBE) using a combination of the integrated mobile technologies (wearable device and phone application) and tailored home-based exercise will be pilot tested. Participants will choose one of the four home-based exercise options \[National Institute of Aging (NIA) Go4Life (an exercise and physical activity campaign from the NIA), Iyengar-style yoga, walking, and modified Otago exercise\] based on participants' preference and goals. The integrated mobile technologies system will allow the investigators to extract heart rate data directly from the wearable device to the research server. This data will be used to provide appropriate and personalized feedback on physical performance. The survey and notification to the participants on the smartphone.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Diabetes | — | UNRESOLVED | — |
| Hypertension | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Tailored Technology-Enhance Home-based exercise program (iHBE) | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- The iHBE program group
- description
- Tailored Technology-Enhance Home-based exercise program (iHBE)
- interventionNames
- Other: Tailored Technology-Enhance Home-based exercise program (iHBE)
- type
- NO_INTERVENTION
- label
- Usual Care (Control group)
- description
- Participants were required to wear physical activity tracker (Fitbit) and respond to the daily symptoms survey (mEMA) while receiving usual care
Primary outcomes (4)
- measure
- Change in Fatigue as Assessed by Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form v1.0-Fatigue 6a
- timeFrame
- Pre- and post-intervention, up to 12 weeks
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria: * participants diagnosed with solid tumor cancer who have completed cancer treatment at least 6 months; * diagnosed with diabetes and/or hypertension for at least a year; * aged 21 years or older, * have an annual household incomes of below $50,000 for families of three, * the average fatigue level within the past 7 days at the level of 3 or more on the 0 (no fatigue) to 10 (worse fatigue) Likert scale * give informed consent. Exclusion Criteria: * currently undergoing treatment for cancer; * have an active infection (e.g., fever, localized redness, swelling, sinus congestion); * diagnosed with a psychological disorder (e.g., suicidal or homicidal tendencies, extreme anxiety or depression)
References
Publications (0)
Data not yet available