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Resilience, PsychologicalLWCSCNCT07087886

Combined Intervention of Long-term Letter Mentoring and Centralized Summer Camp by University Student Volunteers for Disadvantaged Children: A Randomized Controlled Trial

A study testing Combined Resilience Intervention in people with Resilience, Psychological, run by Xiaoxuan Liu.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if a combined intervention of summer camp and letter-writing support works to improve psychological resilience in disadvantaged adolescents in Liangshan, Sichuan. Read more about this study

Who is it for?
Ages 10 to 16 yearsHealthy volunteers can take part
Conditions the study is for
Resilience, Psychological
What is being tested?
Combined Resilience Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
497 participants
Where
No sites listed yet
Study dates
17 Aug 2025to 30 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 16 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Students enrolled in Grade 7 or Grade 8 (junior middle school) in selected schools in Yuexi County, Liangshan Prefecture, Sichuan Province.
  • Identified as "children in adversity," including those from economically disadvantaged families, left-behind children, children with disabilities, or other children deemed at-risk by school officials.
  • Able to understand and complete psychological questionnaires.
  • Mentally and physically able to participate in group activities and engage in written communication.
  • Willing to participate in the study and provide informed assent.
  • Legal guardian has signed written informed consent for participation.

Who cannot join

  • Children with serious psychiatric or developmental disorders (e.g., autism spectrum disorder, intellectual disability) that impair comprehension or participation.
  • Currently receiving professional psychological counseling or treatment that may interfere with the study protocol.
  • Participation in other mental health interventions in the past year.
  • Planning to transfer, drop out, or leave the region during the study period.
  • Judged by the research team to be unsuitable for participation due to medical or other reasons (e.g., serious physical illness that prevents participation in camp activities).

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

xiaoxuan Liu, MA contact

+8613305630831

xiaoxuanliu@zju.edu.cn

Xudong Zhou, PhD contact

+8618158101668

zhouxudong@zju.edu.cn

About this study

The goal of this clinical trial is to learn if a combined intervention of summer camp and letter-writing support works to improve psychological resilience in disadvantaged adolescents in Liangshan, Sichuan. The main questions it aims to answer are:

Does the "summer camp + letter-writing" intervention improve resilience in adolescents who face poverty, lack of parental care, or social risks?

Read more

Does this intervention reduce depression and anxiety symptoms?

Researchers will compare adolescents who join the summer camp and receive monthly letters to those who do not receive this program to see if the intervention helps their mental health and coping skills.

Participants will:

Attend a 5-day summer camp that includes group games, emotion expression activities, life education, and learning support

Receive monthly letters from trained university student volunteers for about 10 months after the camp. The letters will encourage them, give advice, and help them practice what they learned in the camp

Complete surveys about their resilience, depression, and anxiety before the intervention, during it, at the end, and 6 months later

This study will also look at whether the program is cost-effective, meaning if it brings mental health benefits at a reasonable cost.

Read the detailed description

This study will test a new way to help disadvantaged adolescents build psychological resilience. Psychological resilience means having the strength to handle challenges and stress in life. Many adolescents in Liangshan, Sichuan, face poverty, lack of parental care, or social risks, which increase their chances of depression, anxiety, and social withdrawal.

Researchers designed a program with two parts:

Summer camp (first month)

Participants will attend a 5-day summer camp held at a local school. University student volunteers will lead activities such as:

Team-building games to build trust and cooperation

Emotional expression through art, music, and storytelling

Life education and future planning to raise hope and self-confidence

Learning support and academic guidance The camp will provide a safe and supportive environment where adolescents can build positive relationships and learn skills to cope with difficulties.

Letter-writing support (after the camp, for 10 months)

After the summer camp, each participant will be paired with a trained university student volunteer. The volunteer will write a letter to the participant each month. Letters will:

Encourage and support the participant emotionally

Remind them to use the skills learned during the camp

Share stories, advice, and caring words to reduce loneliness

Participants will be randomly assigned to either the intervention group, who will join the camp and receive letters, or the control group, who will continue their normal school life without this program. All participants will complete surveys before the program, halfway through, at the end, and 6 months later to measure:

Psychological resilience

Depression symptoms

Anxiety symptoms

The study will also check if this program is safe, acceptable to adolescents, and cost-effective. There are no known major risks. The program does not replace professional therapy but provides social and emotional support. If any participant shows signs of severe mental health issues, the research team will help them get professional care.

This study aims to find out if combining a short-term camp with long-term letter-writing support can sustainably improve adolescents' mental health in low-resource areas. If proven effective, it may offer a scalable and low-cost way to support disadvantaged youth in rural China.

Being tested
Combined Resilience Intervention
Keywords
Psychological resilience, Disadvantaged adolescents, Letter-writing support, Summer camp intervention, University student volunteers

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Combined Resilience InterventionBehavioural

    A two-phase behavioral intervention aimed at improving psychological resilience among socioeconomically disadvantaged adolescents. The intervention includes:

    1. a 5-day structured summer camp led by trained university student volunteers, featuring psychoeducational group sessions, emotional expression activities, and life skills training, based on SEL, CBT, and positive psychology frameworks; and
    2. a 10-month pen-pal letter-writing component, where each child is matched with a trained university volunteer to receive monthly supportive letters. This stage reinforces the gains from the summer camp through sustained emotional support, skill reminders, and positive guidance.

    The intervention is designed to be low-cost, scalable, and ethically safe, and has been standardized through manuals and training protocols.

Study groups in NCT07087886
Study groupRoleWhat they receive
Intervention GroupExperimentalA two-phase intervention consisting of (1) a 5-day resilience training summer camp and (2) 10-month letter-writing support by university student volunteers.
Receives: Behavioral: Combined Resilience Intervention
Control GroupNo interventionParticipants will not receive the full intervention but will be offered a condensed version after the study ends for ethical consideration.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Psychological resilience (RSCA score) at post-intervention

    Psychological resilience will be assessed using the Resilience Scale for Chinese Adolescents (RSCA), a 27-item validated instrument measuring five dimensions of resilience. Each item is rated on a 5-point Likert scale, and the total score ranges from 27 to 135, with higher scores indicating greater resilience.

    Measured: At baseline (1 month before intervention), mid-intervention (Month 6), end of intervention (Month 11), and follow-up (Month 17)

Secondary outcomes (3)
  1. Change in depressive symptoms from baseline to follow-up (PHQ-9)

    Depressive symptoms will be measured using the 9-item Patient Health Questionnaire (PHQ-9), a validated screening tool for depressive symptoms. Each item is scored from 0 (not at all) to 3 (nearly every day), with a total score range of 0-27. Higher scores indicate more severe depressive symptoms. Clinically significant depression is defined as a score ≥10.

    Measured: At baseline (1 month before intervention), mid-intervention (Month 6), end of intervention (Month 11), and follow-up (Month 17)

  2. Change in anxiety symptoms from baseline to follow-up (GAD-7)

    Anxiety symptoms will be assessed using the 7-item Generalized Anxiety Disorder scale (GAD-7), a validated self-report measure for generalized anxiety. Each item is rated from 0 (not at all) to 3 (nearly every day), with total scores ranging from 0 to 21. A score of ≥10 is considered clinically significant.

    Measured: At baseline (1 month before intervention), mid-intervention (Month 6), end of intervention (Month 11), and follow-up (Month 17)

  3. Change in mobile device addiction symptoms from baseline to follow-up (SAS-SV)

    Digital device addiction will be assessed using the Short Version of the Smartphone Addiction Scale (SAS-SV), adapted for general mobile device use. The scale includes 10 items rated on a 6-point Likert scale (1 = strongly disagree to 6 = strongly agree). Higher scores indicate greater risk of device addiction. A total score above 32 is considered indicative of problematic use.

    Measured: Baseline (T0): 1 month before summer camp Post-intervention (T2): Month 11 Follow-up (T3): Month 17

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Jul 2025
  2. Study start17 Aug 2025 (estimated)
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
497 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07087886
Sponsor's protocol ID
ZGL202506-9
Acronym
LWCSC
Status last verified
Jul 2025
First submitted
16 Jul 2025
Last updated
28 Jul 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: This study involves vulnerable child participants, and individual-level data will not be shared due to ethical and privacy concerns. Only aggregate-level results will be made available in publications or upon request.

Questions about this trial

What is this clinical trial studying?

A study testing Combined Resilience Intervention in people with Resilience, Psychological, run by Xiaoxuan Liu.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 28 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact xiaoxuan Liu, MA (+8613305630831, xiaoxuanliu@zju.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Psychological resilience (RSCA score) at post-intervention (time frame: At baseline (1 month before intervention), mid-intervention (Month 6), end of intervention (Month 11), and follow-up (Month 17)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2025.

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