Group-Based Support Interventions for Adolescents and Young Adults With Lymphoma: A Pilot Randomized Controlled Trial.
무작위 임상시험
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
5 weekly sessions (60 min each) delivered in a group setting via videoconferencing
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Strategies to improve adherence and retention are needed to optimize engagement in this population. [CLINICAL TRIAL REGISTRATION] ClinicalTrials.gov Identifier NCT04270266.
[OBJECTIVE] Lymphomas are one of the primary cancers that affect adolescents and young adults (AYAs).
- 표본수 (n) 28
- p-value p = 0.041
- p-value p = 0.028
APA
Cho D, Ahmed S, et al. (2025). Group-Based Support Interventions for Adolescents and Young Adults With Lymphoma: A Pilot Randomized Controlled Trial.. Psycho-oncology, 34(12), e70343. https://doi.org/10.1002/pon.70343
MLA
Cho D, et al.. "Group-Based Support Interventions for Adolescents and Young Adults With Lymphoma: A Pilot Randomized Controlled Trial.." Psycho-oncology, vol. 34, no. 12, 2025, pp. e70343.
PMID
41298073 ↗
Abstract 한글 요약
[OBJECTIVE] Lymphomas are one of the primary cancers that affect adolescents and young adults (AYAs). We examined the feasibility of two group-based interventions-one meditation-based and one education-based-for AYAs with lymphoma. We also explored their potential benefits for reducing psychological distress and cancer-related symptom burden.
[METHODS] Patients aged 18-39 years with lymphoma undergoing chemotherapy were randomized to either the meditation or psychoeducation intervention. Both received 5 weekly sessions (60 min each) delivered in a group setting via videoconferencing. Participants were assessed at baseline (T1), 6 weeks (T2), and 12 weeks (T3).
[RESULTS] Participants were randomized to the meditation (n = 28) or psychoeducation intervention (n = 32) with a consent rate of 51.4%. Session attendance was similar across interventions, with 60.7% in the meditation intervention and 56.3% in the psychoeducation intervention attending all 5 sessions (χ(4) = 0.65). Assessment completion rates in the meditation intervention were 75% at T2 and 64% at T3; in the psychoeducation intervention, rates were 78% at both time points. From T1 to T3, the psychoeducation intervention showed significant improvements in cancer-related symptom severity (mean difference = 0.75, p = 0.041) and interference (mean difference = 1.07, p = 0.028).
[CONCLUSIONS] Videoconference-delivered, group-based supportive care for AYAs with lymphoma during active cancer treatment appears feasible and may help reduce symptom burden or prevent further worsening of quality of life. Virtual delivery enhances accessibility and scalability across diverse clinical settings. Strategies to improve adherence and retention are needed to optimize engagement in this population.
[CLINICAL TRIAL REGISTRATION] ClinicalTrials.gov Identifier NCT04270266.
[METHODS] Patients aged 18-39 years with lymphoma undergoing chemotherapy were randomized to either the meditation or psychoeducation intervention. Both received 5 weekly sessions (60 min each) delivered in a group setting via videoconferencing. Participants were assessed at baseline (T1), 6 weeks (T2), and 12 weeks (T3).
[RESULTS] Participants were randomized to the meditation (n = 28) or psychoeducation intervention (n = 32) with a consent rate of 51.4%. Session attendance was similar across interventions, with 60.7% in the meditation intervention and 56.3% in the psychoeducation intervention attending all 5 sessions (χ(4) = 0.65). Assessment completion rates in the meditation intervention were 75% at T2 and 64% at T3; in the psychoeducation intervention, rates were 78% at both time points. From T1 to T3, the psychoeducation intervention showed significant improvements in cancer-related symptom severity (mean difference = 0.75, p = 0.041) and interference (mean difference = 1.07, p = 0.028).
[CONCLUSIONS] Videoconference-delivered, group-based supportive care for AYAs with lymphoma during active cancer treatment appears feasible and may help reduce symptom burden or prevent further worsening of quality of life. Virtual delivery enhances accessibility and scalability across diverse clinical settings. Strategies to improve adherence and retention are needed to optimize engagement in this population.
[CLINICAL TRIAL REGISTRATION] ClinicalTrials.gov Identifier NCT04270266.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Female
- Male
- Lymphoma
- Adolescent
- Pilot Projects
- Adult
- Young Adult
- Meditation
- Patient Education as Topic
- Quality of Life
- Psychotherapy
- Group
- Stress
- Psychological
- Psychological Distress
- Feasibility Studies
- AYA cancer survivors
- cancer
- lymphomas
- meditation‐based intervention
- oncology
- psychoeducation
- psychological distress
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