Clinical trial · Interventional
Multicomponent Physical Activity Intervention for the Reduction of Psychosocial Distress in Cancer Patients
Efficacy of an Adapted Multicomponent Physical Activity Intervention to Reduce Psychosocial Distress in Rural Adults Following Cancer Diagnosis
NCT05056831CI-TRIAL-00081880terminatedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): PI Request
Summary
Brief summary (as posted)
This study adapts and assesses the effect of a multicomponent physical activity intervention in reducing psychosocial distress in cancer patients. This study aims to develop a program to help increase physical activity and reduce stress in cancer survivors who live in rural areas.
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 |
|---|---|---|---|
| Anxiety Disorder | — | UNRESOLVED | — |
| Hematopoietic and Lymphoid Cell Neoplasm | Hematopoietic and Lymphoid Cell Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Malignant Solid Neoplasm | Malignant Solid Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (5)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Behavioral Intervention | Behavioral | — | UNRESOLVED |
| Best Practice | Other | — | UNRESOLVED |
| Informational Intervention | Other | — | UNRESOLVED |
| Quality-of-Life Assessment | Other | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Group I (physical activity intervention)
- description
- Patients attend face-to-face mind-body sessions focused on stretching, breathing, and relaxation twice a week and receive targeted text messages daily on their smartphone for 8 weeks.
- interventionNames
- Behavioral: Behavioral Intervention
- Other: Informational Intervention
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
- type
- ACTIVE_COMPARATOR
- label
- Group II (usual care)
- description
- Patients receive usual care.
- interventionNames
- Other: Best Practice
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * PROVIDERS: Work with cancer survivors (e.g., radiation and medical oncologists, oncology nurses, oncology patient navigators, and clinical research coordinators) * PROVIDERS: Place of engagement falls within a rural county in Texas * PROVIDERS: Able to read, speak, and write in English * PROVIDERS: At least 18 years old * PROVIDERS: Have access to a smartphone, tablet, or computer with internet access and willing to attend virtual sessions * INTERVIEW SURVIVORS: Men and women \>= 18 years of age * INTERVIEW SURVIVORS: History of cancer * INTERVIEW SURVIVORS: Currently receiving treatment or have recently completed treatment but are still attending appointments at UTHealth North Campus Tyler (=\< 1 year) * INTERVIEW SURVIVORS: Able to read, speak, and write in English * INTERVIEW SURVIVORS: Have access to a smartphone, tablet, or computer with internet access and willing to attend virtual sessions * INTERVENTION SURVIVORS: Men and women \>= 18 years of age * INTERVENTION SURVIVORS: Received a solid tumor cancer diagnosis stage I-III * INTERVENTION SURVIVORS: Receiving radiation therapy or planning to receive radiation therapy for a solid tumor diagnosis for at least 4 weeks * INTERVENTION SURVIVORS: Able to engage in moderate intensity physical activity as determined by the Physical Activity Readiness Questionnaire (PAR-Q) or by physicians clearance (letter from physician or nurse practitioner) * INTERVENTION SURVIVORS: Physician clearance to participate in the study * INTERVENTION SURVIVORS: Physically inactive (=\< 60 minutes of moderate or greater physical activity \[PA\] per week during the past 6 months) * INTERVENTION SURVIVORS: Live within MD Anderson's rural catchment area * INTERVENTION SURVIVORS: Have a home address where information can be mailed and a working telephone * INTERVENTION SURVIVORS: Have access to a smartphone, tablet, or computer with internet access and willing to attend virtual sessions * INTERVENTION SURVIVORS: Able to read, speak, and write in English * INTERVENTION SURVIVORS: Able to receive text messages on their smartphone (via cellular data or wireless internet) Exclusion Criteria: * PROVIDERS: Does not work with cancer survivors * PROVIDERS: Place of work or engagement falls within an urban/metropolitan county in Texas * PROVIDERS: Does not read, speak, or write in English * PROVIDERS: Below the age of 18 years * INTERVIEW SURVIVORS: No history of cancer * INTERVIEW SURVIVORS: Does not read, speak, or write in English * INTERVIEW SURVIVORS: Below the age of 18 * INTERVENTION SURVIVORS: No history of cancer * INTERVENTION SURVIVORS: Have absolute contraindications to unassisted physical activity (e.g., acute myocardial infarction, severe orthopedic or musculoskeletal limitations) * INTERVENTION SURVIVORS: Currently participating in another intervention to increase physical activity or reduce sedentary behavior * INTERVENTION SURVIVORS: Self-report meeting physical activity recommendations (\>= 60 minutes of moderate or greater PA per week during the past 6 months) * INTERVENTION SURVIVORS: Physical limitations that might be aggravated by participation in moderate-intensity physical activity as measured using the Physical Activity Readiness Questionnaire (PAR-Q), and any physical limitation that prevents engaging in moderate intensity exercise * INTERVENTION SURVIVORS: Primary address falls within an urban/metropolitan county in Texas * INTERVENTION SURVIVORS: Plan to move from the area or discontinue their treatment at UTHealth North Campus Tyler during the 14-week study period * INTERVETION SURVIVORS: Does not read, speak, or write in English * INTERVENTION SURVIVORS: Below the age of 18 * INTERVENTION SURVIVORS: Pregnant or planning to become pregnant during the 14 week study period
References
Publications (0)
Data not yet available
No reference posted for this study.